Stelkast Company
FDA 510(k) & PMA Approved Devices — 40 products
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Total Devices40
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K122883 | EXP TIBIAL INSERTS AND PATELLAR COMPONENTS FOR THE PROVEN GEN-FLEX TOTAL KNEE SYSTEM | JWH | 2013-08-05 | View |
| 510(k) | K122773 | CROSS-OVER ACETABULAR SHELL & LINER | OQG | 2012-10-09 | View |
| 510(k) | K094035 | EXP ACETABULAR LINER, MODELS SC3342 NON-HOODED 28MM, SC3343 HOODED 28MM | OQG | 2011-03-24 | View |
| 510(k) | K081458 | PROVEN STEM EXTENDER | JWH | 2008-06-06 | View |
| 510(k) | K063211 | PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT | JWH | 2007-01-18 | View |
| 510(k) | K051976 | PROVEN REVISION MODULAR TIBIAL TRAY | JWH | 2005-10-17 | View |
| 510(k) | K033944 | STELKAST 32MM MODULAR CERAMIC FEMORAL HEAD | LZO | 2004-03-12 | View |
| 510(k) | K032824 | STELKAST UNICONDYLAR KNEE SYSTEM | HSX | 2003-11-13 | View |
| 510(k) | K031901 | PROVEN REVISION FEMORAL AND PROVEN REVISION TIBIAL INSERT | JWH | 2003-10-10 | View |
| 510(k) | K032110 | PROCLASS PRESS FIT HIP STEM | LWJ | 2003-09-22 | View |
| 510(k) | K030577 | PROVEN MODULAR TIBIAL TRAY | JWH | 2003-03-25 | View |
| 510(k) | K021908 | PROVEN MODULAR POSTERIOR STABILIZED FEMORAL | JWH | 2002-07-09 | View |
| 510(k) | K014049 | EPOCA CODR STEM AND HEAD | KWT | 2002-01-09 | View |
| 510(k) | K010282 | LATERAL OFFSET PROTRACT PRESS FIT HIP STEM | LPH | 2001-02-09 | View |
| 510(k) | K010241 | PROTRACT PRESS FIT HIP STEM-HA COATED | LPH | 2001-02-08 | View |
| 510(k) | K003447 | PROTRACT PRESS FIT HIP STEM | LPH | 2000-12-15 | View |
| 510(k) | K002796 | MODIFICATION TO PROVIDENT HIP SYSTEM | LWJ | 2000-09-28 | View |
| 510(k) | K001984 | PROGENY FORGED COCR CEMENTED FEMORAL COMPONENT | JDG | 2000-09-27 | View |
| 510(k) | K002281 | STELKAST PROVEN KNEE SYSTEM | JWH | 2000-08-17 | View |
| 510(k) | K001745 | MODIFICATION TO PROVIDENT HIP SYSTEM | LWJ | 2000-07-27 | View |
No matching devices.
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