U.S. Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U.S. Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER, CONSENSUS POSTERIOR STABILIZED KNEE, CONSENSUS PCL SUBSITUTING TIBIAL INSERT
24
Total
18
Cleared
0
Denied
U.S. Medical Products, Inc. has 18 FDA 510(k) cleared orthopedic devices. Based in Austin, US.
Historical record: 18 cleared submissions from 1992 to 1996.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - U.S. Medical Products, Inc.
24 devices
Cleared
Aug 15, 1996
CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER
Orthopedic
66d
Cleared
May 22, 1996
CONSENSUS POSTERIOR STABILIZED KNEE
Orthopedic
215d
Cleared
Apr 26, 1996
CONSENSUS PCL SUBSITUTING TIBIAL INSERT
Orthopedic
284d
Cleared
Apr 01, 1996
CONSENSUS ALL POLY TIBIA
Orthopedic
280d
Cleared
Apr 01, 1996
CONSENSUS ACETABULAR SHELL, ALL UHMWPE
Orthopedic
70d
Cleared
Mar 15, 1996
CONSENSUS APEX DOME HOLE PLUG
Orthopedic
51d
Cleared
Feb 21, 1996
CONSENSUS 26MM COCRMO FEMORAL HEAD
Orthopedic
41d
Cleared
Feb 21, 1996
CONSENSUS 32MM COCRMO FEMORAL HEAD
Orthopedic
41d
Cleared
Feb 21, 1996
CONSENSUS 22MM COCRMO FEMORAL HEAD
Orthopedic
28d
Cleared
Feb 20, 1996
CONSENSUS ZIRCONIA FEMORAL HEAD
Orthopedic
90d
Cleared
Nov 06, 1995
CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5
Orthopedic
84d
Cleared
May 31, 1995
CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BASEPLATE
Orthopedic
198d