U.S. Medical Products, Inc.
FDA 510(k) & PMA Approved Devices — 24 products
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Total Devices24
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K962215 | CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER | HWE | 1996-08-15 | View |
| 510(k) | K954818 | CONSENSUS POSTERIOR STABILIZED KNEE | JWH | 1996-05-22 | View |
| 510(k) | K953443 | CONSENSUS PCL SUBSITUTING TIBIAL INSERT | JWH | 1996-04-26 | View |
| 510(k) | K960302 | CONSENSUS ACETABULAR SHELL, ALL UHMWPE | JDI | 1996-04-01 | View |
| 510(k) | K952943 | CONSENSUS ALL POLY TIBIA | JWH | 1996-04-01 | View |
| 510(k) | K960340 | CONSENSUS APEX DOME HOLE PLUG | JDI | 1996-03-15 | View |
| 510(k) | K960156 | CONSENSUS 32MM COCRMO FEMORAL HEAD | JDI | 1996-02-21 | View |
| 510(k) | K960339 | CONSENSUS 22MM COCRMO FEMORAL HEAD | JDI | 1996-02-21 | View |
| 510(k) | K960151 | CONSENSUS 26MM COCRMO FEMORAL HEAD | JDI | 1996-02-21 | View |
| 510(k) | K955386 | CONSENSUS ZIRCONIA FEMORAL HEAD | LZO | 1996-02-20 | View |
| 510(k) | K953792 | CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5 | LZO | 1995-11-06 | View |
| 510(k) | K945589 | CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BASEPLATE | JWH | 1995-05-31 | View |
| 510(k) | K950013 | CONSENSUS(TM) ORTHOPEDIC DRILL BIT | HWE | 1995-05-05 | View |
| 510(k) | K946197 | CONSENSUS(TM) PATELLA REAMER | HWE | 1995-04-05 | View |
| 510(k) | K944946 | CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER | HWE | 1995-02-01 | View |
| 510(k) | K945208 | CONSENSUS HIP SYSTEM -- TROCHANTERIC CUTTER | HWE | 1995-01-27 | View |
| 510(k) | K945189 | CONSENSUS HIP SYSTEM -- CALCAR PLANER | HWE | 1995-01-27 | View |
| 510(k) | K945186 | CONSENUS HIP SYSTEM -- ACETABULAR REAMER | HWE | 1995-01-27 | View |
| 510(k) | K932837 | CONSENSUS KNEE SYSTEM - PRIMARY KNEE | JWH | 1994-09-27 | View |
| 510(k) | K935193 | CONSENSUS HIP SYSTEM- POROUS COATED TITIANIUM FEMORAL STEM | LZO | 1994-08-18 | View |
No matching devices.
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