Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System

Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System is an FDA 510(k)-cleared medical device (K223719) manufactured by Aegis Spine, 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 10, 2023. Regulation: 8.