Xenco Medical CancelleX Cervical Interbody System

Xenco Medical CancelleX Cervical Interbody System is an FDA 510(k)-cleared medical device (K243673) manufactured by Xenco Medical, 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 January 28, 2025. Regulation: 8.