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U.S. Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K962215CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTERAugust 15, 1996
K954818CONSENSUS POSTERIOR STABILIZED KNEEMay 22, 1996
K953443CONSENSUS PCL SUBSITUTING TIBIAL INSERTApril 26, 1996
K960302CONSENSUS ACETABULAR SHELL, ALL UHMWPEApril 1, 1996
K952943CONSENSUS ALL POLY TIBIAApril 1, 1996
K960340CONSENSUS APEX DOME HOLE PLUGMarch 15, 1996
K960156CONSENSUS 32MM COCRMO FEMORAL HEADFebruary 21, 1996
K960339CONSENSUS 22MM COCRMO FEMORAL HEADFebruary 21, 1996
K960151CONSENSUS 26MM COCRMO FEMORAL HEADFebruary 21, 1996
K955386CONSENSUS ZIRCONIA FEMORAL HEADFebruary 20, 1996
K953792CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5November 6, 1995
K945589CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BASEPLATEMay 31, 1995
K950013CONSENSUS(TM) ORTHOPEDIC DRILL BITMay 5, 1995
K946197CONSENSUS(TM) PATELLA REAMERApril 5, 1995
K944946CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMERFebruary 1, 1995
K945189CONSENSUS HIP SYSTEM -- CALCAR PLANERJanuary 27, 1995
K945208CONSENSUS HIP SYSTEM -- TROCHANTERIC CUTTERJanuary 27, 1995
K945186CONSENUS HIP SYSTEM -- ACETABULAR REAMERJanuary 27, 1995
K932837CONSENSUS KNEE SYSTEM - PRIMARY KNEESeptember 27, 1994
K935193CONSENSUS HIP SYSTEM- POROUS COATED TITIANIUM FEMORAL STEMAugust 18, 1994