EVOLUTION MP Revision Femur, EVOLUTION Femoral Augments

EVOLUTION MP Revision Femur, EVOLUTION Femoral Augments is an FDA 510(k)-cleared medical device (K142550) manufactured by Microport Orthopedics, 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 November 6, 2014. Regulation: 8.