
Wrightmedicaltechnologyinc
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INBONE TOTAL ANKLE SYSTEM MODEL 200347902 is an FDA 510(k)-cleared medical device (K103374) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 13, 2010. Regulation: 8.