ADIRA™ Lateral Plate System

ADIRA™ Lateral Plate System is an FDA 510(k)-cleared medical device (K233735) manufactured by Globus Medical, 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 January 24, 2024. Regulation: 8.