
Arthrex, Inc.
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ARTHREX 4.5 MM, 5.5 MM AND 6.5 MM CORKSCREW FT is an FDA 510(k)-cleared medical device (K061665) manufactured by Arthrex, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 24, 2006. Regulation: 8.