EVOLVE EPS ORTHOLOC

EVOLVE EPS ORTHOLOC is an FDA 510(k)-cleared medical device (K102352) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 1, 2010. Regulation: 8.