Depuy, Inc.
FDA 510(k) & PMA Approved Devices — 303 products
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Total Devices303
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K043058 | PINNACLE CONSTRAINED ACETABULAR LINERS | KWZ | 2005-03-14 | View |
| 510(k) | K042664 | LPS UPPER EXTREMITY | JDC | 2004-12-08 | View |
| 510(k) | K041085 | LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY | JWH | 2004-07-22 | View |
| 510(k) | K033959 | LPS | JWH | 2004-07-01 | View |
| 510(k) | K040544 | DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062 | LPH | 2004-05-28 | View |
| 510(k) | K021478 | DELTA SHOULDER | PHX | 2003-11-18 | View |
| 510(k) | K033329 | DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS | HSB | 2003-11-14 | View |
| 510(k) | K032151 | DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS | JWH | 2003-09-26 | View |
| 510(k) | K020541 | AGILITY ANKLE REVISION PROSTHESIS | HSN | 2002-05-20 | View |
| 510(k) | K011810 | ORTHOGENESIS LPS PROXIMAL TIBIAL REPLACEMENT AND ORTHOGENESIS LPS TIBIAL BEARING | KRO | 2001-09-07 | View |
| 510(k) | K003182 | ORTHOGENESIS LPS SYSTEM | JWH | 2001-06-27 | View |
| 510(k) | K001922 | DEPUY NEUFLEX PIP FINGER | KYJ | 2000-08-29 | View |
| 510(k) | K993465 | DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE | HRS | 2000-01-11 | View |
| 510(k) | K991649 | DEPUY ROCKWOOD CLAVICLE PIN | JDW | 1999-07-14 | View |
| 510(k) | K991135 | SOFT TISSUE SUTURE WASHER | HTN | 1999-04-29 | View |
| 510(k) | K984158 | P.F.C. MODULAR PLUS OFFSET TIBIAL TRAY | JWH | 1999-01-28 | View |
| 510(k) | K984378 | DEPUY ACROMED MOSS SPINAL SYSTEM | MNI | 1998-12-30 | View |
| 510(k) | K983583 | DEPUY ACROMED MOSS AND MOSS MIAMI SPINAL SYSTEMS | KWP | 1998-12-03 | View |
| 510(k) | K982330 | DEPUY ORTHOTECH RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT | FTM | 1998-09-25 | View |
| 510(k) | K982511 | DEPUY MOTECH MOSS MIAMI SPINAL SYSTEMS | KWP | 1998-09-14 | View |
No matching devices.
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