MTF Pre-Sutured Tendon

MTF Pre-Sutured Tendon is an FDA 510(k)-cleared medical device (K181633) manufactured by Musculoskeletal Transplant Foundation. 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 March 14, 2019. Regulation: 8.