Dow Corning Wright
FDA 510(k) & PMA Approved Devices — 74 products
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Total Devices74
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K932210 | ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT | JWH | 1994-09-07 | View |
| 510(k) | K932911 | ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT | JWH | 1994-06-30 | View |
| 510(k) | K934354 | LACEY ALL POLYETHYLENE TIBIAL COMPONENT | JWH | 1994-06-03 | View |
| 510(k) | K932222 | SLT FEMORAL HEAD | LZO | 1994-05-27 | View |
| 510(k) | K932858 | ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT | JWH | 1994-02-16 | View |
| 510(k) | K930228 | ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE | JWH | 1993-11-30 | View |
| 510(k) | K925900 | LACEY REVISION FEMORAL COMPONENT | JWH | 1993-08-24 | View |
| 510(k) | K930189 | ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP | JWH | 1993-08-06 | View |
| 510(k) | K930188 | ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT | JWH | 1993-08-03 | View |
| 510(k) | K930190 | ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP | JWH | 1993-08-02 | View |
| 510(k) | K926257 | ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENT | JWH | 1993-05-18 | View |
| 510(k) | K920968 | INFINITY(R) COLLARLESS/MICROTAPER TROCHANTERIC MOD | LZO | 1993-05-05 | View |
| 510(k) | K920929 | POLY INSERT 20 DEGREE | JDL | 1993-05-05 | View |
| 510(k) | K915525 | WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP | JWH | 1993-05-05 | View |
| 510(k) | K920969 | HYDROXYLAPATITE INFINITY(R) | MEH | 1993-05-05 | View |
| 510(k) | K925512 | CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATION | LZO | 1993-02-12 | View |
| 510(k) | K920593 | CERAMIC FEMORAL HEAD | LZO | 1992-08-31 | View |
| 510(k) | K915448 | CORTICAL BONE SCREW | HWC | 1992-02-28 | View |
| 510(k) | K915238 | TRAC-WRIGHT TRAC 10 CATHETER | MCW | 1992-02-19 | View |
| 510(k) | K915350 | HYDROXYAPATITE INFINITY TROCHANTERIC MODULE | MEH | 1992-02-03 | View |
No matching devices.
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