Dow Corning Wright - FDA 510(k) Cleared Devices
74
Total
52
Cleared
0
Denied
Dow Corning Wright has 52 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 52 cleared submissions from 1979 to 1994.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
74 devices
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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