ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201

ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201 is an FDA 510(k)-cleared medical device (K012923) manufactured by Arthrex, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 2001. Regulation: 8.