ORTHOLOC® 3Di Ankle Fracture Plating System

ORTHOLOC® 3Di Ankle Fracture Plating System is an FDA 510(k)-cleared medical device (K163044) 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 January 25, 2017. Regulation: 8.