SpineLinc Anterior Cervical Implant System

SpineLinc Anterior Cervical Implant System is an FDA 510(k)-cleared medical device (K250764) manufactured by Lincotek Medical. 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 4, 2025. Regulation: 8.