Pfizer Hospital Products Group, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K930156 | MEGA PLUS SUPER LAG SCREW | KTT | 1994-02-22 | View |
| 510(k) | K915512 | DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS | JWH | 1992-08-18 | View |
| 510(k) | K920831 | PCA TOTAL HIP SYSTEM (CEMENTLESS USE) | LPH | 1992-06-10 | View |
| 510(k) | K920034 | DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC | JWH | 1992-03-18 | View |
| 510(k) | K915184 | HOWMEDICA ALUMINA FEMORAL HEAD | LZO | 1992-01-31 | View |
| 510(k) | K911656 | PLEUR-EVAC PLUS CONTIN. REINFUS. & AUTOINFUS. SYST | CAC | 1991-08-13 | View |
| 510(k) | K911292 | SCHNEIDER WALLSTENT(R) | FGE | 1991-05-01 | View |
| 510(k) | K905482 | BONDEK POLYGLYCOLIC ACID SYNTHETIC ABSORB. SUTURE | GAM | 1991-03-14 | View |
No matching devices.
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