Trinity™ Dual Mobility System

Trinity™ Dual Mobility System is an FDA 510(k)-cleared medical device (K170359) manufactured by Corin U.S.A. Limited. 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 30, 2017. Regulation: 8.