Republic Spine Restore Cervical Interbody Fusion System

Republic Spine Restore Cervical Interbody Fusion System is an FDA 510(k)-cleared medical device (K190889) manufactured by Republic 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 June 18, 2019. Regulation: 8.