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Alliance Medical Corp.
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ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES is an FDA 510(k)-cleared medical device (K052062) manufactured by Alliance Medical Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 24, 2005. Regulation: 8.