Matira™ Anterior Cervical System

Matira™ Anterior Cervical System is an FDA 510(k)-cleared medical device (K172086) manufactured by Kalitec Direct, 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 21, 2017. Regulation: 8.