Axis Anterior Cervical Plate System

Axis Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K173867) manufactured by Axis Orthopaedics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 4, 2018. Regulation: 8.