Truliant Porous Femoral Components

Truliant Porous Femoral Components is an FDA 510(k)-cleared medical device (K181794) manufactured by Exactech, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 27, 2018. Regulation: 8.