Howmedica Corp. - FDA 510(k) Cleared Devices
373
Total
325
Cleared
0
Denied
Howmedica Corp. has 325 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 325 cleared submissions from 1976 to 1998.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
373 devices
Cleared
Dec 23, 1998
MICRO DYNAMIC MESH
Dental
76d
Cleared
Dec 22, 1998
TYPE 3 FEMORAL COMPONENTS
Orthopedic
85d
Cleared
Dec 16, 1998
DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION
Orthopedic
280d
Cleared
Dec 16, 1998
DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION
Orthopedic
280d
Cleared
Dec 11, 1998
DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
Orthopedic
296d
Cleared
Dec 11, 1998
DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION
Orthopedic
295d
Cleared
Nov 25, 1998
HOFFMANN II MIAMI POST
Orthopedic
57d
Cleared
Nov 20, 1998
ZETA MULTIZONE LOCKING NAIL SYSTEM
Orthopedic
88d
Cleared
Oct 21, 1998
ZETA MULTIZONE SCN LOCKING NAIL
Orthopedic
68d
Cleared
Oct 16, 1998
HOWMEDICA LEIBINGER RESORBABLE FIXATION SYSTEM
Orthopedic
88d
Cleared
Oct 02, 1998
CONTEMPORARY ACETABULAR COMPONENT
Orthopedic
63d
Cleared
Sep 14, 1998
RETROGRADE ROD SYSTEM
Orthopedic
49d
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