FASTAK SUTURE ANCHOR (11.7MM)/(7.5MM)

FASTAK SUTURE ANCHOR (11.7MM)/(7.5MM) is an FDA 510(k)-cleared medical device (K971723) 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 July 29, 1997. Regulation: 8.