Trident Extremity Fixation System

Trident Extremity Fixation System is an FDA 510(k)-cleared medical device (K171690) manufactured by Trident Orthopedics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 2018. Regulation: 8.