FDA 510(k) Applications Submitted by U.S. MEDICAL PRODUCTS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K962215 |
06/10/1996 |
CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER |
U.S. MEDICAL PRODUCTS, INC. |
| K960151 |
01/11/1996 |
CONSENSUS 26MM COCRMO FEMORAL HEAD |
U.S. MEDICAL PRODUCTS, INC. |
| K960156 |
01/11/1996 |
CONSENSUS 32MM COCRMO FEMORAL HEAD |
U.S. MEDICAL PRODUCTS, INC. |
| K960302 |
01/22/1996 |
CONSENSUS ACETABULAR SHELL, ALL UHMWPE |
U.S. MEDICAL PRODUCTS, INC. |
| K960339 |
01/24/1996 |
CONSENSUS 22MM COCRMO FEMORAL HEAD |
U.S. MEDICAL PRODUCTS, INC. |
| K960340 |
01/24/1996 |
CONSENSUS APEX DOME HOLE PLUG |
U.S. MEDICAL PRODUCTS, INC. |
| K952943 |
06/26/1995 |
CONSENSUS ALL POLY TIBIA |
U.S. MEDICAL PRODUCTS, INC. |
| K953443 |
07/17/1995 |
CONSENSUS PCL SUBSITUTING TIBIAL INSERT |
U.S. MEDICAL PRODUCTS, INC. |
| K954818 |
10/20/1995 |
CONSENSUS POSTERIOR STABILIZED KNEE |
U.S. MEDICAL PRODUCTS, INC. |
| K955386 |
11/22/1995 |
CONSENSUS ZIRCONIA FEMORAL HEAD |
U.S. MEDICAL PRODUCTS, INC. |
|
|
