ORTHOLOC® 3Di Ankle Fusion Plating System Line Extension

ORTHOLOC® 3Di Ankle Fusion Plating System Line Extension is an FDA 510(k)-cleared medical device (K163650) 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 April 23, 2017. Regulation: 8.