ARTHREX FIBERWIRE IN USP SIZES

ARTHREX FIBERWIRE IN USP SIZES is an FDA 510(k)-cleared medical device (K021434) 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 November 6, 2002. Regulation: 8.