Xenco Medical Cervical Interbody System (Argus)

Xenco Medical Cervical Interbody System (Argus) is an FDA 510(k)-cleared medical device (K152302) 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 9, 2015. Regulation: 8.