DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM

DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM is an FDA 510(k)-cleared medical device (K990596) manufactured by Avanta Orthopaedics, 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 April 28, 1999. Regulation: 8.