ARTHREX FIBERTAK SUTURE ANCHOR

ARTHREX FIBERTAK SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K140476) 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 August 12, 2014. Regulation: 8.