Smith & Nephew Richards, Inc.
FDA 510(k) & PMA Approved Devices — 87 products
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Total Devices87
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K965224 | EMPOWER ANTERIOR DIRECT SCREWS | KWP | 1997-05-08 | View |
| 510(k) | K963509 | GLOBAL TAPER TAPERED HIP SYSTEM, GT SPECTRON | LPH | 1997-01-27 | View |
| 510(k) | K960444 | FINN ROD TO ROD CONNECTOR | KWP | 1997-01-24 | View |
| 510(k) | K964163 | TRIMAX NAIL SYSTEM | HSB | 1996-12-27 | View |
| 510(k) | K962557 | GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENT | JWH | 1996-12-05 | View |
| 510(k) | K963486 | REVISION HIP SYSTEM | JDI | 1996-11-27 | View |
| 510(k) | K962541 | REFLECTION ACETABULAR REINFORCEMENT RINGS | JDJ | 1996-09-17 | View |
| 510(k) | K962808 | ILIZAROV EXTERNAL FIXATION SYSTEM | KTT | 1996-08-19 | View |
| 510(k) | K962137 | GENESIS II CONSTRAINED SYSTEM | JWH | 1996-08-02 | View |
| 510(k) | K955767 | COFIED MODULAR SHOULDER SYSTEM | KWS | 1996-04-08 | View |
| 510(k) | K960094 | REFLECTION DUAL DIMENSION SHELL | MBL | 1996-03-27 | View |
| 510(k) | K954696 | ROGOZINSKI THORACOLUMBAR SPINAL ROD | KWP | 1996-03-11 | View |
| 510(k) | K953274 | GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM | JWH | 1996-02-05 | View |
| 510(k) | K954909 | PROFIX POSTERIOR-STABILIZED KNEE SYSTEM | JWH | 1996-01-31 | View |
| 510(k) | K955552 | EXPRESSAIRE TORUNIQUET SYSTEM | KCY | 1996-01-05 | View |
| 510(k) | K954491 | HYDROCELL NASAL AND SINUS PACKS | EMX | 1995-11-15 | View |
| 510(k) | K953397 | HEX-FIX FIELD FIXATOR | LXT | 1995-10-31 | View |
| 510(k) | K954712 | INTRAMEDULLARY HIP SCREW (MODIFICATION) | KTT | 1995-10-31 | View |
| 510(k) | K952697 | TITANIUM CLASSIC COMPRESSION HIP SCREW SYSTEM | HWC | 1995-09-12 | View |
| 510(k) | K952271 | GENESIS CONSTRAINED SYSTEM (GCS) | JWH | 1995-09-08 | View |
No matching devices.
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