Anika Tissue Tack Fixation System

Anika Tissue Tack Fixation System is an FDA 510(k)-cleared medical device (K222487) manufactured by Anika Therapeutics, 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 May 7, 2023. Regulation: 8.