ARTHREX DISTAL RADIUS PLATE SYSTEM

ARTHREX DISTAL RADIUS PLATE SYSTEM is an FDA 510(k)-cleared medical device (K131474) manufactured by Arthrex, 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 July 2, 2013. Regulation: 8.