Cervical Interbody and VBR Fusion System

Cervical Interbody and VBR Fusion System is an FDA 510(k)-cleared medical device (K252219) manufactured by Sync Surgical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 13, 2026. Regulation: 8.