Kensey Nash Corp.
FDA 510(k) & PMA Approved Devices — 19 products
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Total Devices19
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103787 | MEDEOR MATRIX | FTM | 2011-02-07 | View |
| 510(k) | K091192 | KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX | NPL | 2009-11-02 | View |
| 510(k) | K091499 | MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY) | FTM | 2009-10-22 | View |
| 510(k) | K090919 | KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANE | NPL | 2009-10-02 | View |
| 510(k) | K073519 | QUICKCAT EXTRACTION CATHETER, MODEL 60090-01 | QEZ | 2008-03-28 | View |
| 510(k) | K071695 | KENSEY NASH MACROPORE SHIELD | FTL | 2007-12-31 | View |
| 510(k) | K072384 | MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE | MQV | 2007-09-21 | View |
| 510(k) | K072195 | THROMCAT THROMBECTOMY CATHETER SYSTEM | MCW | 2007-08-23 | View |
| 510(k) | K071237 | COPIOS BONE VOID FILLER SPONGE AND PASTE | MQV | 2007-06-01 | View |
| 510(k) | K062870 | TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03 | NFA | 2006-10-20 | View |
| 510(k) | K061772 | TRIACTIV FX EMBOLIC PROTECTION SYSTEM | NFA | 2006-07-11 | View |
| 510(k) | K060016 | THROMCAT THROMBECTOMY CATHETER SYSTEM | MCW | 2006-04-25 | View |
| 510(k) | K060092 | QUICKCAT EXTRACTION CATHETER | QEZ | 2006-03-09 | View |
| 510(k) | K043259 | BIOBLANKET SURGICAL MESH | FTM | 2005-08-15 | View |
| 510(k) | K042040 | TRIACTIV SYSTEM | NFA | 2005-03-23 | View |
| 510(k) | K041923 | BIOBLANKET | FTM | 2004-09-08 | View |
| 510(k) | K011943 | IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR | LZN | 2001-09-19 | View |
| 510(k) | K926089 | KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER | GCJ | 1993-07-23 | View |
| 510(k) | K923726 | KENSEY NASH DYNAMIC CLIP SYSTEM | GCJ | 1993-04-06 | View |
No matching devices.
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