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Arthrex, Inc.
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ARTHREX CORKSCREW SUTURE ANCHOR, TAK, AND PUSHLOCK FAMILY is an FDA 510(k)-cleared medical device (K061863) 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 October 18, 2006. Regulation: 8.