Tyber Medical MST Trauma Screw

Tyber Medical MST Trauma Screw is an FDA 510(k)-cleared medical device (K153180) manufactured by Tyber Medical, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 2015. Regulation: 8.