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FDA 510(k), K961433, EBI X FIX DYNAFIX SYSTEM/EBI DFS DISTAL RADIUS FIXATOR SC BONE SCREWS
FDA 510(k), K961433, EBI X FIX DYNAFIX SYSTEM/EBI DFS DISTAL RADIUS FIXATOR SC BONE SCREWS
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510(K) Number: K961433
Device Name: EBI X FIX DYNAFIX SYSTEM/EBI DFS DISTAL RADIUS FIXATOR SC BONE SCREWS
Manufacturer: ELECTRO-BIOLOGY, INC.
Device Classification Name: appliance, fixation, nail/blade/plate combination, multiple component
Regulation Number: 888.3030
Classification Product Code: KTT
Date Received: 04/15/1996
Decision Date: 06/28/1996
Regulation Medical Specialty: Orthopedic
Device Name: EBI X FIX DYNAFIX SYSTEM/EBI DFS DISTAL RADIUS FIXATOR SC BONE SCREWS
Manufacturer: ELECTRO-BIOLOGY, INC.
Device Classification Name: appliance, fixation, nail/blade/plate combination, multiple component
Regulation Number: 888.3030
Classification Product Code: KTT
Date Received: 04/15/1996
Decision Date: 06/28/1996
Regulation Medical Specialty: Orthopedic
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