Medical Device Manufacturer · US , Austin , TX

U.S. Medical Products, Inc. - FDA 510(k) Cleared Devices

24 submissions · 18 cleared · Since 1992

Total

Cleared

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

1-12 of 24

Cleared Aug 15, 1996

CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER

K962215 · HWE

Orthopedic · 66d

Cleared May 22, 1996

CONSENSUS POSTERIOR STABILIZED KNEE

K954818 · JWH

Orthopedic · 215d

Cleared Apr 26, 1996

CONSENSUS PCL SUBSITUTING TIBIAL INSERT

K953443 · JWH

Orthopedic · 284d

Cleared Apr 01, 1996

CONSENSUS ALL POLY TIBIA

K952943 · JWH

Orthopedic · 280d

Cleared Apr 01, 1996

CONSENSUS ACETABULAR SHELL, ALL UHMWPE

K960302 · JDI

Orthopedic · 70d

Cleared Mar 15, 1996

CONSENSUS APEX DOME HOLE PLUG

K960340 · JDI

Orthopedic · 51d

Cleared Feb 21, 1996

CONSENSUS 26MM COCRMO FEMORAL HEAD

K960151 · JDI

Orthopedic · 41d

Cleared Feb 21, 1996

CONSENSUS 32MM COCRMO FEMORAL HEAD

K960156 · JDI

Orthopedic · 41d

Cleared Feb 21, 1996

CONSENSUS 22MM COCRMO FEMORAL HEAD

K960339 · JDI

Orthopedic · 28d

Cleared Feb 20, 1996

CONSENSUS ZIRCONIA FEMORAL HEAD

K955386 · LZO

Orthopedic · 90d

Cleared Nov 06, 1995

CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5

K953792 · LZO

Orthopedic · 84d

Cleared May 31, 1995

CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BASEPLATE

K945589 · JWH

Orthopedic · 198d

U.S. Medical Products, Inc. - FDA 510(k) Cleared Devices

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