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FDA 510(k) K012634, REPROCESSED EXTERNAL FIXATION DEVICE, by Alliance Medical, Inc.

FDA 510(k) K012634, REPROCESSED EXTERNAL FIXATION DEVICE, by Alliance Medical, Inc.

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510(K) Number: K012634
Device Name: REPROCESSED EXTERNAL FIXATION DEVICE
Manufacturer: Alliance Medical, Inc.
Device Classification Name: appliance, fixation, nail/blade/plate combination, single component
Regulation Number: 888.3030
Classification Product Code: KTW
Date Received: 08/13/2001
Decision Date: 06/24/2002
Regulation Medical Specialty: Orthopedic
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