Posterior Fusion Plate, HA Posterior Fusion Plate

Posterior Fusion Plate, HA Posterior Fusion Plate is an FDA 510(k)-cleared medical device (K200066) manufactured by Spinal Simplicity, 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 December 9, 2020. Regulation: 8.