restor3d TiDAL Lumbar Interbody Fusion Device

restor3d TiDAL Lumbar Interbody Fusion Device is an FDA 510(k)-cleared medical device (K220523) manufactured by Restor3D. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 16, 2022. Regulation: 8.