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Conmed Linvatec
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CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503 is an FDA 510(k)-cleared medical device (K101100) manufactured by Conmed Linvatec. 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 25, 2010. Regulation: 8.