dynaMX™ Compression Plate

dynaMX™ Compression Plate is an FDA 510(k)-cleared medical device (K161303) manufactured by Mx Orthopedics, Corp.. 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.