Xenco Medical Posterior Cervical System

Xenco Medical Posterior Cervical System is an FDA 510(k)-cleared medical device (K161478) 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 September 5, 2016. Regulation: 8.