ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM

ANCHORLOK II SOFT TISSUE ANCHOR SYSTEM is an FDA 510(k)-cleared medical device (K963217) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 1, 1996. Regulation: 8.