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FDA 510(k) K011034, SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM, by Synthes (Usa)

FDA 510(k) K011034, SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM, by Synthes (Usa)

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510(K) Number: K011034
Device Name: SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM
Manufacturer: Synthes (Usa)
Device Classification Name: appliance, fixation, nail/blade/plate combination, multiple component
Regulation Number: 888.3030
Classification Product Code: KTT
Date Received: 04/05/2001
Decision Date: 06/27/2001
Regulation Medical Specialty: Orthopedic
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