Osteonics Corp. - FDA 510(k) Cleared Devices
178
Total
136
Cleared
0
Denied
Osteonics Corp. has 136 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 136 cleared submissions from 1980 to 2000.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
178 devices
Cleared
Apr 06, 2000
OSTEONICS SERIES 7000 AD TIBIAL TRAY
Orthopedic
535d
Cleared
Jul 23, 1999
OSTEONICS HA-COATED DEVICES
Orthopedic
561d
Cleared
Apr 30, 1999
OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLY
Orthopedic
144d
Cleared
Mar 25, 1999
OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEM
Orthopedic
227d
Cleared
Feb 24, 1999
OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVE
Orthopedic
62d
Cleared
Feb 18, 1999
OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS
Orthopedic
28d
Cleared
Feb 01, 1999
OSTEONICS COMBINATION SCREW RING/BLOCKER
Orthopedic
13d
Cleared
Dec 18, 1998
OSTEONICS SPINAL SYSTEM CYLINDRICAL BONE SCREWS
Orthopedic
16d
Cleared
Dec 16, 1998
OSTEONICS SECUR-FIT AD GENERATION II ACETABULAR COMPONENT SYSTEM
Orthopedic
71d
Cleared
Dec 16, 1998
OSTEO 9MM IC TIBIAL NAIL
Orthopedic
9d
Cleared
Dec 11, 1998
OSTEONICS HA GENERATION II ACETABULAR COMPONENT SYSTEM
Orthopedic
77d
Cleared
Dec 07, 1998
OSTEO COMPRESSION CONDYLE SCREW SYSTEM
Orthopedic
61d
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