FIBERGRAFT Aeridyan Matrix Bone Graft Substitute

FIBERGRAFT Aeridyan Matrix Bone Graft Substitute is an FDA 510(k)-cleared medical device (K213803) manufactured by Prosidyan, 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 August 22, 2022. Regulation: 8.