DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM

DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM is an FDA 510(k)-cleared medical device (K943853) 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 19, 1995. Regulation: 8.