Skyrim Se Less Intrusive Hud
Less Intrusive Hud Ii Sse
Apr 23, 2013.
So I suspect it has nothing to do with less intrusive HUD. Vampaerr author Jan 6, 2016 @ 2:14pm it shouldn't conflict with iHud, I use it with iHud. If you can't. HDE Number
Approval Date and Docket Number Device Name Company Name and Address Device Description /
Device Indications H170001
8/23/19 Minimally Invasive Deformity Correction (MID-C) System ApiFix, Ltd. Approval for the Minimally Invasive Deformity Correction (MID-C) System. This device is indicated for use in patients with adolescent idiopathic scoliosis (AIS) for treatment of single curves classified as Lenke 1 (thoracic major curve) or Lenke 5 (thoracolumbar/lumbar major curve), having a Cobb angle of 45 to 60 degrees which reduces to less than or equal to 30 degrees on lateral side-bending radiographs, and thoracic kyphosis less than 55 degrees as measured from T5 to T12. H190005
8/16/19 The Tether - Vertebral Body Tethering System Zimmer Biomet Spine, Inc. Approval for The Tether - Vertebral Body Tethering System. This device is indicated for skeletally immature patients that require surgical treatment to obtain and maintain correction of progressive idiopathic scoliosis, with a major Cobb angle of 30 to 65 degrees whose osseous structure is dimensionally adequate to accommodate screw fixation, as determined by radiographic imaging. Patients should have failed bracing and/or be intolerant to brace wear. H180002
5/23/19 NovoTTF-100L System Novocure, Ltd.
Portsmouth, NH03801 Approval for the NovoTTF-100L System. This device is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic, malignant pleural mesothelioma (MPM) to be used concurrently with pemetrexed and platinum-based chemotherapy. H170004
9/14/18 PK Papyrus Covered Coronary Stent System Biotronik, Inc.
Lake Oswego, OR 97035 Approval for the PK Papyrus Covered Coronary Stent System. This device is indicated for the treatment of acute perforations of native coronary arteries and coronary bypass grafts in vessels 2.5 to 5.0 mm in diameter. H170002
3/20/18
75-Day LIPOSORBER LA-15 System Kaneka Pharma America LLC.
Vienna, VA
22180 Approval for the LIPOSORBER LA-15 System to expand the indication to include adult patients with nephrotic syndrome. The LIPOSORBER LA-15 is indicated for use in the treatment of adult and pediatric patients with nephrotic syndrome associated with primary focal segmental glomerulosclerosis, when standard treatment options, including corticosteroid and/or calcineurin inhibitors treatments, are unsuccessful or not well tolerated and the patient has a GFR 60 ml/min/1.73m2 or the patient is post renal transplantation. H160002
6/19/17 PulseRider Aneurysm Neck Reconstruction Device Pulsar Vascular, Inc.
Los Gatos, CA 95032 Approval for the PulseRider Aneurysm Neck Reconstruction Device. This device is indicated for use with neurovascular embolic coils in patients 18 years of age for the treatment of unruptured wide-necked intracranial aneurysms with neck widths 4 mm or dome to neck ratio 2 originating on or near a vessel bifurcation of the basilar tip or carotid terminus with at least a portion of the aneurysm neck overlapping the lumen of the parent artery. The inflow vessels should have diameters from 2.7 mm to 4.5 mm. H150003
5/12/17
75-Day Flourish Pediatric Esophageal Atresia Device Wilson-Cook Medical Inc.
Winston-Salem, NC 27105 Approval for the Flourish Pediatric Esophageal Atresia Device. The Flourish Pediatric Esophageal Atresia Device is indicated for use in lengthening atretic esophageal ends and creating an anastomosis with a non-surgical procedure in pediatric patients, up to one year of age with esophageal atresia without a tracheoesophageal fistula (TEF) or in pediatric patients up to one year of age for whom a concurrent TEF has been closed as a result of a prior procedure. This device is indicated for atretic segments 4cm apart. H070005 1/10/17 AMPLATZER Post-Infarct Muscular VSD Occluder AGA Medical Corporation
5050 Nathan Lane North Plymouth, MN 55442 Approval for the AMPLATZER Post-Infarct Muscular VSD Occluder. The AMPLATZER Post-Infarct Muscular VSD Occluder is a percutaneous transcatheter occlusion device intended for closure of post myocardial infarct muscular ventricular septal defects in patients who are not satisfactory surgical candidates. H130006
12/18/15 FENIX Continence Restoration System Torax Medical, Inc.
Shoreview, MN
55126 Approval for the FENIX Continence Restoration System. This device is indicated for the treatment of fecal incontinence in patients who are not candidates for or have previously failed conservative treatment and less invasive therapy options (e.g. bulking agents, radiofrequency ablation, sacral nerve stimulation). H140005
12/18/15 PDGFRB FISH for Gleevec Eligibility in Myelodysplastic Syndrome / Myeloproliferative Disease (MDS / MPD) ARUP Laboratories
Salt Lake City, UT
84108 Approval for the PDGFRB FISH for Gleevec Eligibility in Myelodysplastic Syndrome/Myeloproliferative Disease (MDS/MPD). This device is indicated for the qualitative detection of PDGFRB gene rearrangement from fresh bone marrow samples of patients with MDS/MPD with a high index of suspicion based on karyotyping showing a 5q3133 anomaly. The PDGFRB FISH assay is indicated as an aid in the selection of MDS/MPD patients for whom Gleevec (imatinib mesylate) treatment is being considered. This assay is for professional use only and is to be performed at a single laboratory site. H140006
12/18/15 KIT D816V Mutation Detection by PCR for Gleevec Eligibility in Aggressive Systemic Mastocytosis (ASM) ARUP Laboratories
Salt Lake City, UT
84108 Approval for the KIT D816V Mutation Detection by PCR for Gleevec Eligibility in Aggressive Systemic Mastocytosis (ASM). KIT D816V Mutation Detection by PCR for Gleevec Eligibility in Aggressive Systemic Mastocytosis (ASM) (referred to as the 'KIT D816V assay') is an in vitro diagnostic test intended for qualitative polymerase chain reaction (PCR) detection of KIT D816V mutational status from fresh bone marrow samples of patients with aggressive systemic mastocytosis. The KIT D816V mutational assay is indicated as an aid in the selection of ASM patients for whom Gleevec (imatinib mesylate) treatment is being considered. This assay is for professional use only and is to be performed at a single laboratory site. H080004
7/16/15
2015-M-2584 Osseoanchored Prostheses for the Rehabilitation of Amputees (OPRA) Device Integrum AB
Alexandria, Virginia
22314
Approval for the Osseoanchored Prostheses for the Rehabilitation of Amputees (OPRA) Device. The OPRA device is indicated for patients who have transfemoral amputation due to trauma or cancer and who have rehabilitation problems with, or cannot use, a conventional socket prosthesis. The OPRA device is intended for skeletally mature patients.
The patient failed to receive benefit from a socket prostheses due to problems such as:
Recurrent skin infections and ulcerations in the socket contact area
Pain
A short stump preventing the use of socket prosthesis
Volume fluctuation in the stump
Soft tissue scarring
Extensive area of skin grafting
Socket retention problems due to excessive perspiration
Restricted mobility H130001
3/5/15 Kaneka Lixelle 2-microglobulin Apheresis Column Kaneka Pharma America, LLC
New York, NY
10036 Approval for the Lixelle 2-microglobulin Apheresis Column (also called the Beta2-Microglobulin Apheresis Column or 2M). This device is indicated for the treatment of patients with clinically diagnosed dialysis-related amyloidosis (DRA). H140001
1/23/15 Impella RP System ABIOMED, Inc.
Danvers, MA 01923 Approval for the Impella RP System. This device is indicated for providing circulatory assistance for up to 14 days in pediatric or adult patients with a body surface area =1.5 m2 who develop acute right heart failure or decompensation following left ventricular assist device implantation, myocardial infarction, heart transplant, or open-heart surgery. H130007
12/12/2014 Barostim neo Legacy System CVRx, Inc.
Minneapolis, MN
55445 Approval for the Barostim neo Legacy System. This device is indicated for use in patients with resistant hypertension who have had bilateral implantation of the Rheos Carotid Sinus Leads Models 1010R, 1010L, 1014L, and 1014R (which have been discontinued and are obsolete) and were determined responders in the Rheos pivotal clinical study. H130004
8/26/2014
2014-M-1280 Pleximmune Plexision Inc
Pittsburg, PA
15224
Approval for Pleximmune. This device is indicated for: The Pleximmune test is intended to be performed at a single laboratory to measure the CD154 expression on T-cytotoxic Memory cells (TcM) in patient's peripheral blood lymphocytes (PBL) isolated from heparinized whole blood (anticoagulant sodium heparin). The Pleximmune test is a qualitative prognostic test intended to be used in patients less than 21 years old with liver or small bowel transplantation. The Pleximmune test is an aid in the evaluation of the risk of acute cellular rejection (ACR) and must be used in conjunction with biopsy, standard clinical assessment and other laboratory information.
The Pleximmune test is intended for use at the following time periods:
Pre-transplantation period: For blood samples collected before transplantation, the test predicts the risk of transplant rejection within 60 days after transplantation; and
Early and late post-transplantation period: For blood samples collected within 60 days (early) after transplantation and for blood samples collected at 200 or more days (late) after transplantation, the test predicts the risk of transplant rejection within 60 days after sampling. H120003
8/12/14
2014-M-1265 XVIVO Perfusion System (XPS) with STEEN Solution Perfusate XVIVO Perfusion, Inc.
Englewood, CO
80110 Approval for the XPS System with STEEN Solution Perfusate. The device is indicated for the flushing and temporary continuous normothermic machine perfusion of initially unacceptable excised donor lungs during which time the ex-vivo function of the lungs can be reassessed for transplantation. H130005
7/25/14
2014-M-1114 Low-Profile Visualized Intraluminal Support Device (LVIS and LVIS Jr.) MicroVention, Inc.
Tustin, CA
92780 Approval for the Low-Profile Visualized Intraluminal Support Device (LVIS and LVIS Jr.). The device is indicated for use with bare platinum embolic coils for the treatment of unruptured, wide-neck (neck 4 mm or dome to neck ratio 2 mm), intracranial, saccular aneurysms arising from a parent vessel with a diameter 2.5 mm and 4.5 mm. H120005
10/10/2013 Kaneka Liposorber LA-15 System Kaneka Pharma America LLC Approval for the Kaneka Liposorber LA-15 System. The device is indicated for use in the treatment of pediatric patients with nephrotic syndrome associated with primary focal segmental glomerulosclerosis, when: 1) Standard treatment options, including corticosteroid and/or calcineurin inhibitors treatments, are unsuccessful or not well tolerated and the patient has a GFR ml/min/1.73m 2 ; or 2) The patient is post renal transplantation. H110002
2/13/2013
FDA-2013-M-0205 Argus II Retinal Prosthesis System Second Sight Medical Products, Inc. This epiretinal prosthesis is surgically implanted in and on the eye and includes an antenna, an electronics case, and an electrode array. The Argus II Retinal Prosthesis System is intended for patients aged 25 years and older with bare or no light perception vision caused by advanced retinitis pigmentosa. H100004
12/16/2011
2011-M-0919 Berlin Heart EXCOR Pediatric Ventricular Assist Device (VAD) Berlin Heart, Inc. The EXCOR is intended to provide mechanical circulatory support as a bridge to cardiac transplantation for pediatric patients. Pediatric candidates with severe isolated left ventricular or biventricular dysfunction who are candidates for cardiac transplant and require circulatory support may be treated using the EXCOR. H090002
11/18/2011
2011-M-0848 BSD-2000 Hyperthermia System BSD Medical Corporation This device is indicated for use in conjunction with radiation therapy for the treatment of cervical carcinoma patients who normally would be treated with combined chemotherapy and radiation but are ineligible for chemotherapy due to patient related factors. H100008
11/01/2011
2011-M-0726 Ovation Abdominal Stent Graft System TriVascular, Inc. The TriVascular Ovation Abdominal Stent Graft System is indicated in subjects diagnosed with an aneurysm in the abdominal aorta with small aortic diameters and access vessels of less than 7 mm in diameter, and having vascular morphology suitable for endovascular repair. NOTE: This HDE is superseded by PMA P120006 H100006
09/28/2011
2011-M-0707 NeuRx DPS, Diaphragm Pacing System Synapse Biomedical, Inc. The NeuRx Diaphragm Pacing System (DPS) is a percutaneous, intramuscular, diaphragm motor point stimulating device intended for use in amyotrophic lateral sclerosis (ALS) patients with a stimulatable diaphragm (both right and left portions) as demonstrated by voluntary contraction or phrenic nerve conduction studies, and who are experiencing chronic hypoventilation (CH) , but not progressed to an FVC less than 45 predicted. For use only in patients 21 years of age or older. H100002
04/01/2011
2011-M-0241 cPAX Aneurysm Treatment System NeuroVasx, Inc. The cPAX Aneurysm Treatment System is indicated for use in the adult population (22 years of age and older) for the treatment of wide-necked large and giant-sized cerebral aneurysms (10) mm that require use of adjunctive assist-devices such as stents or balloons. H080005
03/10/2011
11M-0170 Elana Surgical Kit HUD Elana, Inc. The Elana Surgical KitHUD, when connected to the Spectranetics Xenon-Chloride Laser Model CVX-300, is indicated for creating arteriotomies during an intracranial vascular bypass procedure in patients 13 years of age or older with an aneurysm or a skull base tumor affecting a large ( 2.5 mm), intracranial artery that failed balloon test occlusion, cannot be sacrificed, or cannot be treated with conventional means due to local anatomy or complexity. H080002
25-Jan-2010
10M-0063 Medtronic Melody Transcatheter Pulmonary Valve (Model PB10) and Medtronic Ensemble Transcatheter Valve Delivery System (NU10) Medtronic, Inc.
This device is indicated for use as an adjunct to
surgery in the management of pediatric and adult patients with the following clinical conditions:
Existence of a full (circumferential) RVOT conduit that was equal to or greater than 16 mm
in diameter when originally implanted and
Dysfunctional Right Ventricular Outflow Tract (RVOT) conduits with a clinical indication
for intervention, and either:
Regurgitation: moderate regurgitation, or
Stenosis: mean RVOT gradient 35 mmHg.
NOTE: This HDE is superseded by PMA P140017. H050003
19-Feb-2009
09M-0090 Reclaim Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD) Therapy Medtronic Neuromodulation This device is indicated for bilateral stimulation of the anterior limb of the internal capsule, AIC, as an adjunct to medications and as an alternative to anterior capsulotomy for treatment of chronic, severe, treatment-resistant obsessive compulsive disorder (OCD) in adult patients who have failed at least three selective serotonin reuptake inhibitors (SSRIs). H060002
24-Oct-2008
08M-0579 IBV Valve System Spiration, Inc. This device is indicated to control prolonged air leaks of the lung, or significant air leaks that are likely to become prolonged air leaks, following lobectomy, segmentectomy, or lung volume reduction surgery (LVRS). An air leak present on post-operative day 7 is considered prolonged unless present only during forced exhalation or cough. An air leak present on day 5 should be considered for treatment if it is: 1) continuous, 2) present during normal inhalation phase of inspiration, or 3) present upon normal expiration and accompanied by subcutaneous emphysema or respiratory compromise. IBV Valve System use is limited to 6 weeks per prolonged air leak. H040004
10-Oct-2008
08M-0562 INFUSE/MASTERGRAFT Posterolateral Revision Device Medtronic Sofamor Danek USA, Inc. This device has been withdrawn at the request of the sponsor effective March 23, 2010. H070004
07-Oct-2008
08M-0563 Levitronix Centrimag Right Ventricular Assist System (RVAS) Levitronix, LLC This device is indicated for temporary circulatory support for up to 14 days for patients in cardiogenic shock due to acute right ventricular failure. H070003
17-Jun-2008
08M-0378 NeuRx RA/4 Synapse Biomedical, Inc. This device is indicated for use in patients with stable, high spinal cord injuries with stimulatable diaphragms, but lack control of their diaphragms. The device is indicated to allow the patients to breathe without the assistance of a mechanical ventilator for at least 4 continuous hours a day. For use only in patients 18 years of age or older. H990002
25-Oct-2007
07M-0415 Epicel (cultured epidermal autografts) Genzyme Biosurgery The device is indicated for use in patients who have deep dermal or full thickness burns comprising a total body surface area of greater than or equal to 30. It may be used in conjunction with split-thickness autografts, or alone in patients for whom split-thickness autografts may not be an option due to the severity and extent of their burns. Jurisdiction for this product has been transferred to CBER. H060001
08-May-2007
07M-0190 ENTERPRISE Vascular Reconstruction Device and Delivery System Cordis Neurovascular, Inc. Use with embolic coils for the treatment of wide-neck, intracranial, saccular or fusiform aneurysms arising from a parent vessel with a diameter of = 3 mm and = 4 mm. Wide-neck is defined as having a neck width = 4mm or a dome-to-neck ratio 2. H060003
11-Apr-2007
07M-0156 Onyx Liquid Embolic System (Onyx HD-500, Model 105-8101-500) EV3 Neurovascular Treatment of intracranial, saccular, sidewall aneurysms that present with a wide neck (= 4 mm) or with a dome-to-neck ratio 2 that are not amenable to treatment with surgical clipping. H060004
24-Jan-2007
07M-0038 Fujirebio Mesomark Assay Fujirebio Diagnostics, Inc. The Fujirebio Diagnostics, Inc. (FDI) MESOMARK is an Enzyme Linked Immunosorbent Assay (ELISA) for the quantitative measurement of Soluble Mesothelin Related Peptides (SMRP) in human serum. Measurement of SMRP may aid in the monitoring of patients diagnosed with epitheloid or biphasic mesothelioma. MESOMARK values must be interpreted in conjunction with all other available clinical laboratory data. H040006
05-Sep-2006
06M-0368 Abiocor Implantable Replacement Heart Abiomed, Inc.
This device is indicated for use in severe biventricular end stage heart disease patients who are not cardiac transplant candidates and who
are less than 75 years old,
require multiple inotropic support,
are not treatable by LVAD destination therapy, and
are not weanable from biventricular support if on such support. H040005
31-Mar-2006
06M-0163 Karl Storz Semi-Rigid TTTS Fetoscopy Instrument Set, Karl Storz Rigid TTTS Fetoscopy Instrument Set with 0 or 12 degree scope, and Karl Storz Rigid TTTS Fetoscopy Instrument Set with 30 degree scope Karl Storz Endoscopy-America, Inc. The Karl Storz TTTS Fetoscopy Instruments Sets are indicated for selective laser photocoagulation (S-PLC) in the treatment of twin-to-twin transfusion syndrome (TTTS) for fetuses whose gestational age is between 16 and 26 weeks. H050001
03-Aug-2005
05M-0308 Wingspan Stent System with Gateway PTA Balloon Catheter Boston Scientific Smart This device is indicated for improving cerebral artery lumen diameter in patients with intracranial atherosclerotic disease, refractory to medical therapy, in intracranial vessels with greater than or equal to 50 stenosis that are accessible to the system. H030005
30-Mar-2005
05M-0132 CoAxia NeuroFlo Catheter CoAxia, Inc. This device is indicated for the treatment of cerebral ischemia resulting from symptomatic vasospasm following aneurismal subarachnoid hemorrhage, secured by either surgical or endovascular intervention for patients who have failed maximal medical management. H030009
24-Aug-2004
04M-0415 Vertical Expandable Prosthetic Titanium Rib (VEPTR) Synthes (USA)
For the treatment of Thoracic Insufficiency Syndrome (TIS) in skeletally immature patients. TIS is defined as the inability of the thorax to support normal respiration or lung growth. For the purpose of identifying potential TIS patients, the categories in which TIS patients fall are as follows:
Flail Chest Syndrome
Rib fusion and scoliosis
Hypoplastic thorax syndrome, including
Jeune's syndrome
Achondroplasia
Jarcho-Levin syndrome
Ellis van Creveld syndrome
NOTE: This HDE is superseded by 510(k) K142587. H040002
26-Jul-2004
06M-0233 INTACS Prescription Inserts for Keratoconus (0.25mm, 0.30mm, and 0.35mm) Addition Technology
INTACS prescription inserts are intended for the reduction or elimination of myopia and astigmatism in patients with keratoconus, who are no longer able to achieve adequate vision with their contact lenses or spectacles, so that their functional vision may be restored and the need for a corneal transplant procedure may potentially be deferred.
The specific subset of keratoconic patients proposed to be treated with INTACS prescription inserts are those patients:
who have experienced a progressive deterioration in their vision, such that they can no longer achieve adequate functional vision on a daily basis with their contact lenses or spectacles;
who are 21 years of age or older;
who have clear central corneas;
who have a corneal thickness of 450 microns or greater at the proposed incision site; and
who have corneal transplantation as the only remaining option to improve their functional vision. H020008
07-Apr-2004
04M-0165 OP-1 Putty Stryker Biotech
35 South Street
Hopkinton, MA 01748 For use as an alternative to autograft in compromised patients requiring revision posterolateral (intertransverse) lumbar spinal fusion, for whom autologous bone and bone marrow harvest are not feasible or are not expected to promote fusion. Examples of compromising factors include osteoporosis, smoking and diabetes. H030003
25-Feb-2004
04M-0090 DeBakey VAD Child Left Ventricular Assist System MicroMed Technology, Inc. For use to provide temporary left side mechanical circulatory support as a bridge to cardiac transplantation for pediatric patients (5-16 years old, with BSA= 0.7 m 2 and 1.5 2 ) who are in NYHA Class IV end stage heart failure, are refractory to medical therapy and who are (listed) candidates for cardiac transplantation. H030004
24-Feb-2004
04M-0084 Heartsbreath Menssana Research Inc.
1 Horizon Road
Suite 1415
Fort Lee, NJ 07024-6510
USA For use as an aid in the diagnosis of grade 3 heart transplant rejection in patients who have received heart transplants within the preceding year. The Heartsbreath test is intended to be used as an adjunct to, and not as a substitute for, endomyocardial biopsy. The use of the device is limited to patients who have had endomyocardial biopsy within the previous month. H020003
21-Nov-2003
03M-0536 CONTEGRA Pulmonary Valved Conduit Medtronic, Inc The CONTEGRA Pulmonary Valved Conduit is indicated for correction or reconstruction of the Right Ventricular Outflow Tract (RVOT) in patients aged less than 18 years with any of the following congenital heart malformations:
Pulmonary Stenosis
Tetralogy of Fallot
Truncus Arteriosus
Transposition with Ventricular Septal Defect (VSD)
Pulmonary Atresia In addition, the conduit is indicated for the replacement of previously implanted, but dysfunctional, pulmonary homografts or valved conduits. H020004
07-Jul-2003
03M-0305 Dermagraft Smith and Nephew Wound Management This device has been withdrawn by the sponsor as of September 28, 2007. Jurisdiction for this product has been transferred to CBER. H020007
15-Apr-2003
03M-0157 Medtronic Activa Dystonia Therapy Medtronic Neurological For unilateral or bilateral stimulation of the internal globus pallidus (GPi) or the subthalamic nucleus (STN) to aid in the management of chronic, intractable (drug refractory) primary dystonia, including generalized and/or segmental dystonia, hemidystonia, and cervical dystonia (torticollis) in patients seven years of age or above H020002
02-Sep-2002
02M-0409 Neuroform Microdelivery Stent System SMART Therapeutics, Inc.
2551 Merced St.
San Leandro, CA 94577
USA The Neuroform Microdelivery Stent System is intended for use with embolic coils for the treatment of wide neck, intracranial, saccular aneurysms arising from a parent vessel with a diameter of greater than or equal to 2mm and less than or equal to 4.5mm that are not amenable to treatment with surgical clipping. Wide neck aneurysms are defined as having a neck of 4mm or a dome-to-neck ratio of H010004
09-Aug-2002
02M-0361 NEUROLINK System, including NEUROLINK Stent Delivery Catheter and NEUROLINK Balloon Dilatation Catheter Guidant Corporation
Santa Clara, CA USA The NEUROLINK System is indicated for the treatment of patients with recurrent intracranial stroke attributable to atherosclerotic disease refractory to medical therapy in intracranial vessels ranging from 2.5 to 4.5 mm in diameter with 50 stenosis and that are accessible to the stent system H000007
05-Apr-2002
02M-0167 Amplatzer PFO Occluder AGA Medical Corporation
Golden Valley, MN This document has been withdrawn as of October 31, 2006. For more information, please visit this link. H010005
22-Mar-2002
02M-0121 Ascension PIP Ascension Orthopedics, Inc.
Austin, TX For use in arthroplasty of the proximal interphalangeal (PIP) joint when the patients has soft tissue and bone that can provide adequate stabilization and fixation under high demand loading conditions after reconstruction; and needs a revision of a failed PIP prostheis, or has pain, limited motion, or joint subluxation/dislocation secondary to damage or destruction of the articular cartilage. H000002
19-Dec-2001
02M-0311 VISX Excimer Laser System and Custom Contoured Ablation Pattern (C-CAP) Method VISX, Inc. For the treatment of asymmetrical ablation patterns from previous laser refractive surgery caused by decentration of the treatment as viewed on the Zeiss Humphrey topography unit and treated with the STAR S3 ActiveTrak Excimer Laser System in patients:
who exhibit symptomatology supportive of visual defect: reduced best spectacle-corrected visual acuity, debilitating glare, monocular diplopia (double vision), and/or debilitating halos; and,
who pre-operatively have at least a 6 m difference on the elevation topography, from the lowest point to the highest point, over a 6.5 mm diameter or over the patients pupil diameter as measured by the Zeiss Humphrey topographer, whichever is larger H010002
17-Oct-2001
01M-0482 OP-1 Implant Stryker Biotech
Hopkinton, MA The device is indicated for use as an alternative to autograph in recalcitrant long bone nonunions where use of autograph is unfeasible and alternative treatments have failed. H010001
28-Aug-2001
01M-0392 Avanta Metacarpophalangeal (MCP) Joint Implant Finger Prosthesis Avanta Orthopaedics, Inc.
San Diego, CA The device is indicated for use in arthroplasty of the MCP joint when either the:
patient is in need of a revision of failed MCP prosthesis(es); or
patient expects to place his/her hands under loading situations which preclude the use of an alternative implant in the painful osteo-arthritic and post traumatic MCP joint. H000004
19-Mar-2001
01M-0485 PROSTALAC Hip Temporary Prosthesis DePuy Orthopaedics, Inc., a Johnson Johnson Company This device is indicated for use as a short-term total hip replacement (THR) in patients who need a two-stage procedure to treat a confirmed infection of their THR and where vancomycin and tobramycin are the most appropriate antibiotics for treatment of the infection based on the susceptibility pattern of the infecting microorganism(s). H990013
21-Feb-2001
01M-0201 Composite Cultured Skin (CCS) Ortec International, Inc.
New York, NY 10032 For use in patients with mitten hand deformities due to Recessive Dystrophic Epidermolysis Bullosa (RDEB) as an adjunct to standard autograft procedures (i.e., skin grafts and flaps) for covering wounds and donor sites created after the surgical release of hand contractures (i.e., mitten hand deformities). Jurisdiction for this product has been transferred to CBER. H000001
10-Jan-2001
010M-006 JOMED JOSTENT Coronary Stent Graft JOMED AB For Use in the treatment of free perforations, defined as free contrast extravasation into the pericardium, in native coronary vessels or saphenous vein bypass grafts 2.75 mm in diameter. H990012
11-May-2000
00M-1354 TAS Ecarin Clotting Time Test Cardiovascular Diagnostics, Inc. To be used to determine the anticoagulant effect of recombinant hirudin (r-hirudin) during cardiopulmonary bypass in patients who have heparin induced thrombocytopenia (HIT). H990014
31-Mar-2000
00M-1451 Enterra Therapy System (formerly named Gastric Electrical Stimulation (GES) System Medtronic, Inc. For the treatment of chronic, intractable (drug refractory) nausea and vomiting secondary to gastroparesis of diabetic or idiopathic etiology. H990008
09-Mar-2000
00M-1228 Telescopic Plate Spacer (TPS) Spinal System Interpore Cross International
The sponsor has withdrawn this HDE effective Sept. 1, 2010 H990011
01-Feb-2000
00M-0599 CardioSEAL Septal Occlusion System Nitinol Medical Technologies, Inc This document has been withdrawn as of October 31, 2006. For more information, please visit this link. H980006
10-Dec-1999
99M-5539 TheraSphere MDS Nordion, Inc.,
Kanata, Ontario, Canada For radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable hepatocellular carcinoma (HCC) who can have placement of appropriately positioned hepatic arterial catheters. H990007
07-Dec-1999
99M-5327 BioGlueSurgical Adhesive CryoLife, Inc. For use as an adjunct in the surgical repair of acute thoracic aortic dissections. NOTE: This HDE is superseded by PMA P010003. H980007
30-Sep-1999
99M-4810 Shelhigh Pulmonic Valve Conduit Model NR-4000 with 'No-React' Treatment Shelhigh, Inc. For replacement of the diseased, damaged. or absent pulmonic artery in small children or infants up to age 4 years, with Transposition of the Great Arteries, Truncus Arteriosis, Tetrology of Fallot with associated cardiac anomalies or with Pulmonary Atresia, or replacement of failed conduits in young patients with accelerated conduit failure. H990005
28-Sep-1999
99M-4763 CardioSEALSeptal Occlusion System Nitinol Medical Technologies, Inc For the treatment of patients with complex ventricular septal defects (VSD) of a significant size to warrant closure, but that, based on location, cannot be closed with standard surgical transatrial or transarterial approaches. H990003
20-Sep-1999
99M-4619 ActiconNeosphincter American Medical Systems, Inc. For the treatment of severe fecal incontinence in post-pubescent males and females who have failed, or are not candidates for, less invasive forms of restorative therapy. H990004
08-Sep-1999
99M-4134 CardioSEAL Septal Occlusion System Nitinol Medical Technologies, Inc. For the treatment of patients with complex single ventricle physiology who have undergone a fenestrated Fontan palliation procedure and require closure of the fenestration. H980008
19-Feb-1999
99M-0255 VOCARE Bladder System NeuroControl Corporation
Valley View, OH 44125 For the treatment of patients who have clinically complete spinal cord lesions (ASIA Classification) with intact parasympathetic innervation of the bladder and are skeletally mature and neurologically stable, to provide urination on demand and to reduce post-void residual volumes of urine. Secondary intended use is to aid in bowel evacuation H980005
28-Dec-1998
99M-0150 VOCARE Bladder System NeuroControl Corp.
Valley View, OH 44125 For the treatment of patients who have clinically complete spinal cord lesions (ASIA Classification) with intact parasympathetic innervation of the bladder and are skeletally mature and neurologically stable, to provide urination on demand and to reduce post-void residual volumes of urine. H980002
28-Sep-1998
98M-0895 Avanta Proximal Interphalangeal (PIP) Finger Prosthesis Avanta Orthopaedics, Inc For use in arthroplasty of the PIP joint when either the: (1) patient is in need of a revision of failed PIP prosthesis(es); or (2) patient expects to place his/her hands under loading situations which preclude the use of an alternative implant in the painful osteo-arthritic and post traumaic arthritic PIP joint. H970005
30-Apr-1998
98M-0452 Perma-Flow Coronary Graft, Model 2C10 Possis Medical, Inc.
Minneapolis, MN 55433 For single or multiple vessel coronary artery bypass in patients who are receiving coronary bypass grafting but who have inadequate autologous conduit to complete the required revascularization. H970004
06-Apr-1998
98M-0435 Excorim Immunoadsorption System Cobe BCT., Inc.
Lakewood, CO 80215 For use in the treatment of patients with hemophhilia A and B who have Factor VIII or Factor IX inhibitor titers above 10 Bethesda Units/ml (BU/ml). The purpose of the system is to lower the inhibitor levels so that routine clotting factor rerplacement therapy can be considered. It may be used in an acute setting (to control bleeding during an acute hemmorrhage or for emergency surgery) or as a preventive measure to prepare patients for elective surgery. H970003
16-Dec-1997
98M-0163 Urostim William E. Kaplan, M.D. and Ingrid Richards, R.N., MSN
Chicago, IL 60614 For use in children for the treatment of neurogenic bladder disease secondary to spina bifida H970001
30-Sep-1997
98M-0164 King's College Hospital (KCH) Fetal Bladder Drainage Catheter Rocket Medical PLC
England For urinary tract decompression following the diagnosis of post-vesicular obstructive uropathy in fetuses 18 to 32 weeks gestational age H960001
14-Feb-1997
97M-0124 Harrison Fetal Bladder Stent Set (Lowery Modification) Cook OB/GYN
Spencer, IN 47460 For fetal urinary tract decompression following the diagnosis of fetal post-vesicular obstructive uropathy in fetuses of 18 to 32 weeks gestational age
Less Intrusive HUD II (with Customization) Description Discussions 0 Comments 51 Change Notes 51 Comments Colonel Jim May 25, 2018 @ 9:48am Nexus mod is down for moderation, is there any comment on this? Arimoryx Apr 20, 2018 @ 2:57pm Mod doesn't not work (2018). For latest version check skyrim nexus, less intrusive hud II. Calendyn Oct 19, 2013 @ 2:37pm I'm thoroughly enjoying the mod, especially the sneak bar-it's a dramatic improvement over the vanilla. Page 1 of 29 - Less Intrusive HUD II SE - posted in File topics: Less Intrusive HUD II SELess Intrusive HUD II allows you to tweak / change pretty much every element in the vanilla HUD And it does so: IN GAME! No seperate.txt files, no more going in/out game to check your setting. Skyrim Se Less Intrusive Hud Less Intrusive Hud Ii Sse
Regulated Product(s) Topic(s)
Less Intrusive Hud Ii Sse
Apr 23, 2013.
So I suspect it has nothing to do with less intrusive HUD. Vampaerr author Jan 6, 2016 @ 2:14pm it shouldn't conflict with iHud, I use it with iHud. If you can't. HDE Number
Approval Date and Docket Number Device Name Company Name and Address Device Description /
Device Indications H170001
8/23/19 Minimally Invasive Deformity Correction (MID-C) System ApiFix, Ltd. Approval for the Minimally Invasive Deformity Correction (MID-C) System. This device is indicated for use in patients with adolescent idiopathic scoliosis (AIS) for treatment of single curves classified as Lenke 1 (thoracic major curve) or Lenke 5 (thoracolumbar/lumbar major curve), having a Cobb angle of 45 to 60 degrees which reduces to less than or equal to 30 degrees on lateral side-bending radiographs, and thoracic kyphosis less than 55 degrees as measured from T5 to T12. H190005
8/16/19 The Tether - Vertebral Body Tethering System Zimmer Biomet Spine, Inc. Approval for The Tether - Vertebral Body Tethering System. This device is indicated for skeletally immature patients that require surgical treatment to obtain and maintain correction of progressive idiopathic scoliosis, with a major Cobb angle of 30 to 65 degrees whose osseous structure is dimensionally adequate to accommodate screw fixation, as determined by radiographic imaging. Patients should have failed bracing and/or be intolerant to brace wear. H180002
5/23/19 NovoTTF-100L System Novocure, Ltd.
Portsmouth, NH03801 Approval for the NovoTTF-100L System. This device is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic, malignant pleural mesothelioma (MPM) to be used concurrently with pemetrexed and platinum-based chemotherapy. H170004
9/14/18 PK Papyrus Covered Coronary Stent System Biotronik, Inc.
Lake Oswego, OR 97035 Approval for the PK Papyrus Covered Coronary Stent System. This device is indicated for the treatment of acute perforations of native coronary arteries and coronary bypass grafts in vessels 2.5 to 5.0 mm in diameter. H170002
3/20/18
75-Day LIPOSORBER LA-15 System Kaneka Pharma America LLC.
Vienna, VA
22180 Approval for the LIPOSORBER LA-15 System to expand the indication to include adult patients with nephrotic syndrome. The LIPOSORBER LA-15 is indicated for use in the treatment of adult and pediatric patients with nephrotic syndrome associated with primary focal segmental glomerulosclerosis, when standard treatment options, including corticosteroid and/or calcineurin inhibitors treatments, are unsuccessful or not well tolerated and the patient has a GFR 60 ml/min/1.73m2 or the patient is post renal transplantation. H160002
6/19/17 PulseRider Aneurysm Neck Reconstruction Device Pulsar Vascular, Inc.
Los Gatos, CA 95032 Approval for the PulseRider Aneurysm Neck Reconstruction Device. This device is indicated for use with neurovascular embolic coils in patients 18 years of age for the treatment of unruptured wide-necked intracranial aneurysms with neck widths 4 mm or dome to neck ratio 2 originating on or near a vessel bifurcation of the basilar tip or carotid terminus with at least a portion of the aneurysm neck overlapping the lumen of the parent artery. The inflow vessels should have diameters from 2.7 mm to 4.5 mm. H150003
5/12/17
75-Day Flourish Pediatric Esophageal Atresia Device Wilson-Cook Medical Inc.
Winston-Salem, NC 27105 Approval for the Flourish Pediatric Esophageal Atresia Device. The Flourish Pediatric Esophageal Atresia Device is indicated for use in lengthening atretic esophageal ends and creating an anastomosis with a non-surgical procedure in pediatric patients, up to one year of age with esophageal atresia without a tracheoesophageal fistula (TEF) or in pediatric patients up to one year of age for whom a concurrent TEF has been closed as a result of a prior procedure. This device is indicated for atretic segments 4cm apart. H070005 1/10/17 AMPLATZER Post-Infarct Muscular VSD Occluder AGA Medical Corporation
5050 Nathan Lane North Plymouth, MN 55442 Approval for the AMPLATZER Post-Infarct Muscular VSD Occluder. The AMPLATZER Post-Infarct Muscular VSD Occluder is a percutaneous transcatheter occlusion device intended for closure of post myocardial infarct muscular ventricular septal defects in patients who are not satisfactory surgical candidates. H130006
12/18/15 FENIX Continence Restoration System Torax Medical, Inc.
Shoreview, MN
55126 Approval for the FENIX Continence Restoration System. This device is indicated for the treatment of fecal incontinence in patients who are not candidates for or have previously failed conservative treatment and less invasive therapy options (e.g. bulking agents, radiofrequency ablation, sacral nerve stimulation). H140005
12/18/15 PDGFRB FISH for Gleevec Eligibility in Myelodysplastic Syndrome / Myeloproliferative Disease (MDS / MPD) ARUP Laboratories
Salt Lake City, UT
84108 Approval for the PDGFRB FISH for Gleevec Eligibility in Myelodysplastic Syndrome/Myeloproliferative Disease (MDS/MPD). This device is indicated for the qualitative detection of PDGFRB gene rearrangement from fresh bone marrow samples of patients with MDS/MPD with a high index of suspicion based on karyotyping showing a 5q3133 anomaly. The PDGFRB FISH assay is indicated as an aid in the selection of MDS/MPD patients for whom Gleevec (imatinib mesylate) treatment is being considered. This assay is for professional use only and is to be performed at a single laboratory site. H140006
12/18/15 KIT D816V Mutation Detection by PCR for Gleevec Eligibility in Aggressive Systemic Mastocytosis (ASM) ARUP Laboratories
Salt Lake City, UT
84108 Approval for the KIT D816V Mutation Detection by PCR for Gleevec Eligibility in Aggressive Systemic Mastocytosis (ASM). KIT D816V Mutation Detection by PCR for Gleevec Eligibility in Aggressive Systemic Mastocytosis (ASM) (referred to as the 'KIT D816V assay') is an in vitro diagnostic test intended for qualitative polymerase chain reaction (PCR) detection of KIT D816V mutational status from fresh bone marrow samples of patients with aggressive systemic mastocytosis. The KIT D816V mutational assay is indicated as an aid in the selection of ASM patients for whom Gleevec (imatinib mesylate) treatment is being considered. This assay is for professional use only and is to be performed at a single laboratory site. H080004
7/16/15
2015-M-2584 Osseoanchored Prostheses for the Rehabilitation of Amputees (OPRA) Device Integrum AB
Alexandria, Virginia
22314
Approval for the Osseoanchored Prostheses for the Rehabilitation of Amputees (OPRA) Device. The OPRA device is indicated for patients who have transfemoral amputation due to trauma or cancer and who have rehabilitation problems with, or cannot use, a conventional socket prosthesis. The OPRA device is intended for skeletally mature patients.
The patient failed to receive benefit from a socket prostheses due to problems such as:
Recurrent skin infections and ulcerations in the socket contact area
Pain
A short stump preventing the use of socket prosthesis
Volume fluctuation in the stump
Soft tissue scarring
Extensive area of skin grafting
Socket retention problems due to excessive perspiration
Restricted mobility H130001
3/5/15 Kaneka Lixelle 2-microglobulin Apheresis Column Kaneka Pharma America, LLC
New York, NY
10036 Approval for the Lixelle 2-microglobulin Apheresis Column (also called the Beta2-Microglobulin Apheresis Column or 2M). This device is indicated for the treatment of patients with clinically diagnosed dialysis-related amyloidosis (DRA). H140001
1/23/15 Impella RP System ABIOMED, Inc.
Danvers, MA 01923 Approval for the Impella RP System. This device is indicated for providing circulatory assistance for up to 14 days in pediatric or adult patients with a body surface area =1.5 m2 who develop acute right heart failure or decompensation following left ventricular assist device implantation, myocardial infarction, heart transplant, or open-heart surgery. H130007
12/12/2014 Barostim neo Legacy System CVRx, Inc.
Minneapolis, MN
55445 Approval for the Barostim neo Legacy System. This device is indicated for use in patients with resistant hypertension who have had bilateral implantation of the Rheos Carotid Sinus Leads Models 1010R, 1010L, 1014L, and 1014R (which have been discontinued and are obsolete) and were determined responders in the Rheos pivotal clinical study. H130004
8/26/2014
2014-M-1280 Pleximmune Plexision Inc
Pittsburg, PA
15224
Approval for Pleximmune. This device is indicated for: The Pleximmune test is intended to be performed at a single laboratory to measure the CD154 expression on T-cytotoxic Memory cells (TcM) in patient's peripheral blood lymphocytes (PBL) isolated from heparinized whole blood (anticoagulant sodium heparin). The Pleximmune test is a qualitative prognostic test intended to be used in patients less than 21 years old with liver or small bowel transplantation. The Pleximmune test is an aid in the evaluation of the risk of acute cellular rejection (ACR) and must be used in conjunction with biopsy, standard clinical assessment and other laboratory information.
The Pleximmune test is intended for use at the following time periods:
Pre-transplantation period: For blood samples collected before transplantation, the test predicts the risk of transplant rejection within 60 days after transplantation; and
Early and late post-transplantation period: For blood samples collected within 60 days (early) after transplantation and for blood samples collected at 200 or more days (late) after transplantation, the test predicts the risk of transplant rejection within 60 days after sampling. H120003
8/12/14
2014-M-1265 XVIVO Perfusion System (XPS) with STEEN Solution Perfusate XVIVO Perfusion, Inc.
Englewood, CO
80110 Approval for the XPS System with STEEN Solution Perfusate. The device is indicated for the flushing and temporary continuous normothermic machine perfusion of initially unacceptable excised donor lungs during which time the ex-vivo function of the lungs can be reassessed for transplantation. H130005
7/25/14
2014-M-1114 Low-Profile Visualized Intraluminal Support Device (LVIS and LVIS Jr.) MicroVention, Inc.
Tustin, CA
92780 Approval for the Low-Profile Visualized Intraluminal Support Device (LVIS and LVIS Jr.). The device is indicated for use with bare platinum embolic coils for the treatment of unruptured, wide-neck (neck 4 mm or dome to neck ratio 2 mm), intracranial, saccular aneurysms arising from a parent vessel with a diameter 2.5 mm and 4.5 mm. H120005
10/10/2013 Kaneka Liposorber LA-15 System Kaneka Pharma America LLC Approval for the Kaneka Liposorber LA-15 System. The device is indicated for use in the treatment of pediatric patients with nephrotic syndrome associated with primary focal segmental glomerulosclerosis, when: 1) Standard treatment options, including corticosteroid and/or calcineurin inhibitors treatments, are unsuccessful or not well tolerated and the patient has a GFR ml/min/1.73m 2 ; or 2) The patient is post renal transplantation. H110002
2/13/2013
FDA-2013-M-0205 Argus II Retinal Prosthesis System Second Sight Medical Products, Inc. This epiretinal prosthesis is surgically implanted in and on the eye and includes an antenna, an electronics case, and an electrode array. The Argus II Retinal Prosthesis System is intended for patients aged 25 years and older with bare or no light perception vision caused by advanced retinitis pigmentosa. H100004
12/16/2011
2011-M-0919 Berlin Heart EXCOR Pediatric Ventricular Assist Device (VAD) Berlin Heart, Inc. The EXCOR is intended to provide mechanical circulatory support as a bridge to cardiac transplantation for pediatric patients. Pediatric candidates with severe isolated left ventricular or biventricular dysfunction who are candidates for cardiac transplant and require circulatory support may be treated using the EXCOR. H090002
11/18/2011
2011-M-0848 BSD-2000 Hyperthermia System BSD Medical Corporation This device is indicated for use in conjunction with radiation therapy for the treatment of cervical carcinoma patients who normally would be treated with combined chemotherapy and radiation but are ineligible for chemotherapy due to patient related factors. H100008
11/01/2011
2011-M-0726 Ovation Abdominal Stent Graft System TriVascular, Inc. The TriVascular Ovation Abdominal Stent Graft System is indicated in subjects diagnosed with an aneurysm in the abdominal aorta with small aortic diameters and access vessels of less than 7 mm in diameter, and having vascular morphology suitable for endovascular repair. NOTE: This HDE is superseded by PMA P120006 H100006
09/28/2011
2011-M-0707 NeuRx DPS, Diaphragm Pacing System Synapse Biomedical, Inc. The NeuRx Diaphragm Pacing System (DPS) is a percutaneous, intramuscular, diaphragm motor point stimulating device intended for use in amyotrophic lateral sclerosis (ALS) patients with a stimulatable diaphragm (both right and left portions) as demonstrated by voluntary contraction or phrenic nerve conduction studies, and who are experiencing chronic hypoventilation (CH) , but not progressed to an FVC less than 45 predicted. For use only in patients 21 years of age or older. H100002
04/01/2011
2011-M-0241 cPAX Aneurysm Treatment System NeuroVasx, Inc. The cPAX Aneurysm Treatment System is indicated for use in the adult population (22 years of age and older) for the treatment of wide-necked large and giant-sized cerebral aneurysms (10) mm that require use of adjunctive assist-devices such as stents or balloons. H080005
03/10/2011
11M-0170 Elana Surgical Kit HUD Elana, Inc. The Elana Surgical KitHUD, when connected to the Spectranetics Xenon-Chloride Laser Model CVX-300, is indicated for creating arteriotomies during an intracranial vascular bypass procedure in patients 13 years of age or older with an aneurysm or a skull base tumor affecting a large ( 2.5 mm), intracranial artery that failed balloon test occlusion, cannot be sacrificed, or cannot be treated with conventional means due to local anatomy or complexity. H080002
25-Jan-2010
10M-0063 Medtronic Melody Transcatheter Pulmonary Valve (Model PB10) and Medtronic Ensemble Transcatheter Valve Delivery System (NU10) Medtronic, Inc.
This device is indicated for use as an adjunct to
surgery in the management of pediatric and adult patients with the following clinical conditions:
Existence of a full (circumferential) RVOT conduit that was equal to or greater than 16 mm
in diameter when originally implanted and
Dysfunctional Right Ventricular Outflow Tract (RVOT) conduits with a clinical indication
for intervention, and either:
Regurgitation: moderate regurgitation, or
Stenosis: mean RVOT gradient 35 mmHg.
NOTE: This HDE is superseded by PMA P140017. H050003
19-Feb-2009
09M-0090 Reclaim Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD) Therapy Medtronic Neuromodulation This device is indicated for bilateral stimulation of the anterior limb of the internal capsule, AIC, as an adjunct to medications and as an alternative to anterior capsulotomy for treatment of chronic, severe, treatment-resistant obsessive compulsive disorder (OCD) in adult patients who have failed at least three selective serotonin reuptake inhibitors (SSRIs). H060002
24-Oct-2008
08M-0579 IBV Valve System Spiration, Inc. This device is indicated to control prolonged air leaks of the lung, or significant air leaks that are likely to become prolonged air leaks, following lobectomy, segmentectomy, or lung volume reduction surgery (LVRS). An air leak present on post-operative day 7 is considered prolonged unless present only during forced exhalation or cough. An air leak present on day 5 should be considered for treatment if it is: 1) continuous, 2) present during normal inhalation phase of inspiration, or 3) present upon normal expiration and accompanied by subcutaneous emphysema or respiratory compromise. IBV Valve System use is limited to 6 weeks per prolonged air leak. H040004
10-Oct-2008
08M-0562 INFUSE/MASTERGRAFT Posterolateral Revision Device Medtronic Sofamor Danek USA, Inc. This device has been withdrawn at the request of the sponsor effective March 23, 2010. H070004
07-Oct-2008
08M-0563 Levitronix Centrimag Right Ventricular Assist System (RVAS) Levitronix, LLC This device is indicated for temporary circulatory support for up to 14 days for patients in cardiogenic shock due to acute right ventricular failure. H070003
17-Jun-2008
08M-0378 NeuRx RA/4 Synapse Biomedical, Inc. This device is indicated for use in patients with stable, high spinal cord injuries with stimulatable diaphragms, but lack control of their diaphragms. The device is indicated to allow the patients to breathe without the assistance of a mechanical ventilator for at least 4 continuous hours a day. For use only in patients 18 years of age or older. H990002
25-Oct-2007
07M-0415 Epicel (cultured epidermal autografts) Genzyme Biosurgery The device is indicated for use in patients who have deep dermal or full thickness burns comprising a total body surface area of greater than or equal to 30. It may be used in conjunction with split-thickness autografts, or alone in patients for whom split-thickness autografts may not be an option due to the severity and extent of their burns. Jurisdiction for this product has been transferred to CBER. H060001
08-May-2007
07M-0190 ENTERPRISE Vascular Reconstruction Device and Delivery System Cordis Neurovascular, Inc. Use with embolic coils for the treatment of wide-neck, intracranial, saccular or fusiform aneurysms arising from a parent vessel with a diameter of = 3 mm and = 4 mm. Wide-neck is defined as having a neck width = 4mm or a dome-to-neck ratio 2. H060003
11-Apr-2007
07M-0156 Onyx Liquid Embolic System (Onyx HD-500, Model 105-8101-500) EV3 Neurovascular Treatment of intracranial, saccular, sidewall aneurysms that present with a wide neck (= 4 mm) or with a dome-to-neck ratio 2 that are not amenable to treatment with surgical clipping. H060004
24-Jan-2007
07M-0038 Fujirebio Mesomark Assay Fujirebio Diagnostics, Inc. The Fujirebio Diagnostics, Inc. (FDI) MESOMARK is an Enzyme Linked Immunosorbent Assay (ELISA) for the quantitative measurement of Soluble Mesothelin Related Peptides (SMRP) in human serum. Measurement of SMRP may aid in the monitoring of patients diagnosed with epitheloid or biphasic mesothelioma. MESOMARK values must be interpreted in conjunction with all other available clinical laboratory data. H040006
05-Sep-2006
06M-0368 Abiocor Implantable Replacement Heart Abiomed, Inc.
This device is indicated for use in severe biventricular end stage heart disease patients who are not cardiac transplant candidates and who
are less than 75 years old,
require multiple inotropic support,
are not treatable by LVAD destination therapy, and
are not weanable from biventricular support if on such support. H040005
31-Mar-2006
06M-0163 Karl Storz Semi-Rigid TTTS Fetoscopy Instrument Set, Karl Storz Rigid TTTS Fetoscopy Instrument Set with 0 or 12 degree scope, and Karl Storz Rigid TTTS Fetoscopy Instrument Set with 30 degree scope Karl Storz Endoscopy-America, Inc. The Karl Storz TTTS Fetoscopy Instruments Sets are indicated for selective laser photocoagulation (S-PLC) in the treatment of twin-to-twin transfusion syndrome (TTTS) for fetuses whose gestational age is between 16 and 26 weeks. H050001
03-Aug-2005
05M-0308 Wingspan Stent System with Gateway PTA Balloon Catheter Boston Scientific Smart This device is indicated for improving cerebral artery lumen diameter in patients with intracranial atherosclerotic disease, refractory to medical therapy, in intracranial vessels with greater than or equal to 50 stenosis that are accessible to the system. H030005
30-Mar-2005
05M-0132 CoAxia NeuroFlo Catheter CoAxia, Inc. This device is indicated for the treatment of cerebral ischemia resulting from symptomatic vasospasm following aneurismal subarachnoid hemorrhage, secured by either surgical or endovascular intervention for patients who have failed maximal medical management. H030009
24-Aug-2004
04M-0415 Vertical Expandable Prosthetic Titanium Rib (VEPTR) Synthes (USA)
For the treatment of Thoracic Insufficiency Syndrome (TIS) in skeletally immature patients. TIS is defined as the inability of the thorax to support normal respiration or lung growth. For the purpose of identifying potential TIS patients, the categories in which TIS patients fall are as follows:
Flail Chest Syndrome
Rib fusion and scoliosis
Hypoplastic thorax syndrome, including
Jeune's syndrome
Achondroplasia
Jarcho-Levin syndrome
Ellis van Creveld syndrome
NOTE: This HDE is superseded by 510(k) K142587. H040002
26-Jul-2004
06M-0233 INTACS Prescription Inserts for Keratoconus (0.25mm, 0.30mm, and 0.35mm) Addition Technology
INTACS prescription inserts are intended for the reduction or elimination of myopia and astigmatism in patients with keratoconus, who are no longer able to achieve adequate vision with their contact lenses or spectacles, so that their functional vision may be restored and the need for a corneal transplant procedure may potentially be deferred.
The specific subset of keratoconic patients proposed to be treated with INTACS prescription inserts are those patients:
who have experienced a progressive deterioration in their vision, such that they can no longer achieve adequate functional vision on a daily basis with their contact lenses or spectacles;
who are 21 years of age or older;
who have clear central corneas;
who have a corneal thickness of 450 microns or greater at the proposed incision site; and
who have corneal transplantation as the only remaining option to improve their functional vision. H020008
07-Apr-2004
04M-0165 OP-1 Putty Stryker Biotech
35 South Street
Hopkinton, MA 01748 For use as an alternative to autograft in compromised patients requiring revision posterolateral (intertransverse) lumbar spinal fusion, for whom autologous bone and bone marrow harvest are not feasible or are not expected to promote fusion. Examples of compromising factors include osteoporosis, smoking and diabetes. H030003
25-Feb-2004
04M-0090 DeBakey VAD Child Left Ventricular Assist System MicroMed Technology, Inc. For use to provide temporary left side mechanical circulatory support as a bridge to cardiac transplantation for pediatric patients (5-16 years old, with BSA= 0.7 m 2 and 1.5 2 ) who are in NYHA Class IV end stage heart failure, are refractory to medical therapy and who are (listed) candidates for cardiac transplantation. H030004
24-Feb-2004
04M-0084 Heartsbreath Menssana Research Inc.
1 Horizon Road
Suite 1415
Fort Lee, NJ 07024-6510
USA For use as an aid in the diagnosis of grade 3 heart transplant rejection in patients who have received heart transplants within the preceding year. The Heartsbreath test is intended to be used as an adjunct to, and not as a substitute for, endomyocardial biopsy. The use of the device is limited to patients who have had endomyocardial biopsy within the previous month. H020003
21-Nov-2003
03M-0536 CONTEGRA Pulmonary Valved Conduit Medtronic, Inc The CONTEGRA Pulmonary Valved Conduit is indicated for correction or reconstruction of the Right Ventricular Outflow Tract (RVOT) in patients aged less than 18 years with any of the following congenital heart malformations:
Pulmonary Stenosis
Tetralogy of Fallot
Truncus Arteriosus
Transposition with Ventricular Septal Defect (VSD)
Pulmonary Atresia In addition, the conduit is indicated for the replacement of previously implanted, but dysfunctional, pulmonary homografts or valved conduits. H020004
07-Jul-2003
03M-0305 Dermagraft Smith and Nephew Wound Management This device has been withdrawn by the sponsor as of September 28, 2007. Jurisdiction for this product has been transferred to CBER. H020007
15-Apr-2003
03M-0157 Medtronic Activa Dystonia Therapy Medtronic Neurological For unilateral or bilateral stimulation of the internal globus pallidus (GPi) or the subthalamic nucleus (STN) to aid in the management of chronic, intractable (drug refractory) primary dystonia, including generalized and/or segmental dystonia, hemidystonia, and cervical dystonia (torticollis) in patients seven years of age or above H020002
02-Sep-2002
02M-0409 Neuroform Microdelivery Stent System SMART Therapeutics, Inc.
2551 Merced St.
San Leandro, CA 94577
USA The Neuroform Microdelivery Stent System is intended for use with embolic coils for the treatment of wide neck, intracranial, saccular aneurysms arising from a parent vessel with a diameter of greater than or equal to 2mm and less than or equal to 4.5mm that are not amenable to treatment with surgical clipping. Wide neck aneurysms are defined as having a neck of 4mm or a dome-to-neck ratio of H010004
09-Aug-2002
02M-0361 NEUROLINK System, including NEUROLINK Stent Delivery Catheter and NEUROLINK Balloon Dilatation Catheter Guidant Corporation
Santa Clara, CA USA The NEUROLINK System is indicated for the treatment of patients with recurrent intracranial stroke attributable to atherosclerotic disease refractory to medical therapy in intracranial vessels ranging from 2.5 to 4.5 mm in diameter with 50 stenosis and that are accessible to the stent system H000007
05-Apr-2002
02M-0167 Amplatzer PFO Occluder AGA Medical Corporation
Golden Valley, MN This document has been withdrawn as of October 31, 2006. For more information, please visit this link. H010005
22-Mar-2002
02M-0121 Ascension PIP Ascension Orthopedics, Inc.
Austin, TX For use in arthroplasty of the proximal interphalangeal (PIP) joint when the patients has soft tissue and bone that can provide adequate stabilization and fixation under high demand loading conditions after reconstruction; and needs a revision of a failed PIP prostheis, or has pain, limited motion, or joint subluxation/dislocation secondary to damage or destruction of the articular cartilage. H000002
19-Dec-2001
02M-0311 VISX Excimer Laser System and Custom Contoured Ablation Pattern (C-CAP) Method VISX, Inc. For the treatment of asymmetrical ablation patterns from previous laser refractive surgery caused by decentration of the treatment as viewed on the Zeiss Humphrey topography unit and treated with the STAR S3 ActiveTrak Excimer Laser System in patients:
who exhibit symptomatology supportive of visual defect: reduced best spectacle-corrected visual acuity, debilitating glare, monocular diplopia (double vision), and/or debilitating halos; and,
who pre-operatively have at least a 6 m difference on the elevation topography, from the lowest point to the highest point, over a 6.5 mm diameter or over the patients pupil diameter as measured by the Zeiss Humphrey topographer, whichever is larger H010002
17-Oct-2001
01M-0482 OP-1 Implant Stryker Biotech
Hopkinton, MA The device is indicated for use as an alternative to autograph in recalcitrant long bone nonunions where use of autograph is unfeasible and alternative treatments have failed. H010001
28-Aug-2001
01M-0392 Avanta Metacarpophalangeal (MCP) Joint Implant Finger Prosthesis Avanta Orthopaedics, Inc.
San Diego, CA The device is indicated for use in arthroplasty of the MCP joint when either the:
patient is in need of a revision of failed MCP prosthesis(es); or
patient expects to place his/her hands under loading situations which preclude the use of an alternative implant in the painful osteo-arthritic and post traumatic MCP joint. H000004
19-Mar-2001
01M-0485 PROSTALAC Hip Temporary Prosthesis DePuy Orthopaedics, Inc., a Johnson Johnson Company This device is indicated for use as a short-term total hip replacement (THR) in patients who need a two-stage procedure to treat a confirmed infection of their THR and where vancomycin and tobramycin are the most appropriate antibiotics for treatment of the infection based on the susceptibility pattern of the infecting microorganism(s). H990013
21-Feb-2001
01M-0201 Composite Cultured Skin (CCS) Ortec International, Inc.
New York, NY 10032 For use in patients with mitten hand deformities due to Recessive Dystrophic Epidermolysis Bullosa (RDEB) as an adjunct to standard autograft procedures (i.e., skin grafts and flaps) for covering wounds and donor sites created after the surgical release of hand contractures (i.e., mitten hand deformities). Jurisdiction for this product has been transferred to CBER. H000001
10-Jan-2001
010M-006 JOMED JOSTENT Coronary Stent Graft JOMED AB For Use in the treatment of free perforations, defined as free contrast extravasation into the pericardium, in native coronary vessels or saphenous vein bypass grafts 2.75 mm in diameter. H990012
11-May-2000
00M-1354 TAS Ecarin Clotting Time Test Cardiovascular Diagnostics, Inc. To be used to determine the anticoagulant effect of recombinant hirudin (r-hirudin) during cardiopulmonary bypass in patients who have heparin induced thrombocytopenia (HIT). H990014
31-Mar-2000
00M-1451 Enterra Therapy System (formerly named Gastric Electrical Stimulation (GES) System Medtronic, Inc. For the treatment of chronic, intractable (drug refractory) nausea and vomiting secondary to gastroparesis of diabetic or idiopathic etiology. H990008
09-Mar-2000
00M-1228 Telescopic Plate Spacer (TPS) Spinal System Interpore Cross International
The sponsor has withdrawn this HDE effective Sept. 1, 2010 H990011
01-Feb-2000
00M-0599 CardioSEAL Septal Occlusion System Nitinol Medical Technologies, Inc This document has been withdrawn as of October 31, 2006. For more information, please visit this link. H980006
10-Dec-1999
99M-5539 TheraSphere MDS Nordion, Inc.,
Kanata, Ontario, Canada For radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable hepatocellular carcinoma (HCC) who can have placement of appropriately positioned hepatic arterial catheters. H990007
07-Dec-1999
99M-5327 BioGlueSurgical Adhesive CryoLife, Inc. For use as an adjunct in the surgical repair of acute thoracic aortic dissections. NOTE: This HDE is superseded by PMA P010003. H980007
30-Sep-1999
99M-4810 Shelhigh Pulmonic Valve Conduit Model NR-4000 with 'No-React' Treatment Shelhigh, Inc. For replacement of the diseased, damaged. or absent pulmonic artery in small children or infants up to age 4 years, with Transposition of the Great Arteries, Truncus Arteriosis, Tetrology of Fallot with associated cardiac anomalies or with Pulmonary Atresia, or replacement of failed conduits in young patients with accelerated conduit failure. H990005
28-Sep-1999
99M-4763 CardioSEALSeptal Occlusion System Nitinol Medical Technologies, Inc For the treatment of patients with complex ventricular septal defects (VSD) of a significant size to warrant closure, but that, based on location, cannot be closed with standard surgical transatrial or transarterial approaches. H990003
20-Sep-1999
99M-4619 ActiconNeosphincter American Medical Systems, Inc. For the treatment of severe fecal incontinence in post-pubescent males and females who have failed, or are not candidates for, less invasive forms of restorative therapy. H990004
08-Sep-1999
99M-4134 CardioSEAL Septal Occlusion System Nitinol Medical Technologies, Inc. For the treatment of patients with complex single ventricle physiology who have undergone a fenestrated Fontan palliation procedure and require closure of the fenestration. H980008
19-Feb-1999
99M-0255 VOCARE Bladder System NeuroControl Corporation
Valley View, OH 44125 For the treatment of patients who have clinically complete spinal cord lesions (ASIA Classification) with intact parasympathetic innervation of the bladder and are skeletally mature and neurologically stable, to provide urination on demand and to reduce post-void residual volumes of urine. Secondary intended use is to aid in bowel evacuation H980005
28-Dec-1998
99M-0150 VOCARE Bladder System NeuroControl Corp.
Valley View, OH 44125 For the treatment of patients who have clinically complete spinal cord lesions (ASIA Classification) with intact parasympathetic innervation of the bladder and are skeletally mature and neurologically stable, to provide urination on demand and to reduce post-void residual volumes of urine. H980002
28-Sep-1998
98M-0895 Avanta Proximal Interphalangeal (PIP) Finger Prosthesis Avanta Orthopaedics, Inc For use in arthroplasty of the PIP joint when either the: (1) patient is in need of a revision of failed PIP prosthesis(es); or (2) patient expects to place his/her hands under loading situations which preclude the use of an alternative implant in the painful osteo-arthritic and post traumaic arthritic PIP joint. H970005
30-Apr-1998
98M-0452 Perma-Flow Coronary Graft, Model 2C10 Possis Medical, Inc.
Minneapolis, MN 55433 For single or multiple vessel coronary artery bypass in patients who are receiving coronary bypass grafting but who have inadequate autologous conduit to complete the required revascularization. H970004
06-Apr-1998
98M-0435 Excorim Immunoadsorption System Cobe BCT., Inc.
Lakewood, CO 80215 For use in the treatment of patients with hemophhilia A and B who have Factor VIII or Factor IX inhibitor titers above 10 Bethesda Units/ml (BU/ml). The purpose of the system is to lower the inhibitor levels so that routine clotting factor rerplacement therapy can be considered. It may be used in an acute setting (to control bleeding during an acute hemmorrhage or for emergency surgery) or as a preventive measure to prepare patients for elective surgery. H970003
16-Dec-1997
98M-0163 Urostim William E. Kaplan, M.D. and Ingrid Richards, R.N., MSN
Chicago, IL 60614 For use in children for the treatment of neurogenic bladder disease secondary to spina bifida H970001
30-Sep-1997
98M-0164 King's College Hospital (KCH) Fetal Bladder Drainage Catheter Rocket Medical PLC
England For urinary tract decompression following the diagnosis of post-vesicular obstructive uropathy in fetuses 18 to 32 weeks gestational age H960001
14-Feb-1997
97M-0124 Harrison Fetal Bladder Stent Set (Lowery Modification) Cook OB/GYN
Spencer, IN 47460 For fetal urinary tract decompression following the diagnosis of fetal post-vesicular obstructive uropathy in fetuses of 18 to 32 weeks gestational age
Less Intrusive HUD II (with Customization) Description Discussions 0 Comments 51 Change Notes 51 Comments Colonel Jim May 25, 2018 @ 9:48am Nexus mod is down for moderation, is there any comment on this? Arimoryx Apr 20, 2018 @ 2:57pm Mod doesn't not work (2018). For latest version check skyrim nexus, less intrusive hud II. Calendyn Oct 19, 2013 @ 2:37pm I'm thoroughly enjoying the mod, especially the sneak bar-it's a dramatic improvement over the vanilla. Page 1 of 29 - Less Intrusive HUD II SE - posted in File topics: Less Intrusive HUD II SELess Intrusive HUD II allows you to tweak / change pretty much every element in the vanilla HUD And it does so: IN GAME! No seperate.txt files, no more going in/out game to check your setting. Skyrim Se Less Intrusive Hud Less Intrusive Hud Ii Sse
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