VyPlate Anterior Cervical Plate System

VyPlate Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K221572) manufactured by Vy Spine, LLC. 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 25, 2022. Regulation: 8.