Medical Device Manufacturer · US , Mchenry , IL

Dow Corning Wright - FDA 510(k) Cleared Devices

74 submissions · 52 cleared · Since 1979

74

Total

52

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dow Corning Wright Orthopedic ✕

64 devices

1-12 of 64

Cleared Sep 07, 1994

ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT

Orthopedic · 488d

Cleared Jun 30, 1994

ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT

Orthopedic · 379d

Cleared Jun 03, 1994

LACEY ALL POLYETHYLENE TIBIAL COMPONENT

Orthopedic · 269d

Cleared May 27, 1994

SLT FEMORAL HEAD

Orthopedic · 385d

Cleared Feb 16, 1994

ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT

Orthopedic · 251d

Cleared Nov 30, 1993

ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE

Orthopedic · 315d

Cleared Aug 24, 1993

LACEY REVISION FEMORAL COMPONENT

Orthopedic · 277d

Cleared Aug 06, 1993

ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP

Orthopedic · 204d

Cleared Aug 03, 1993

ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT

Orthopedic · 201d

Cleared Aug 02, 1993

ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP

Orthopedic · 200d

Cleared May 18, 1993

ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENT

Orthopedic · 151d

Cleared May 05, 1993

WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP

Orthopedic · 512d

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