Magnes-C Anterior Cervical Plate System

Magnes-C Anterior Cervical Plate System is an FDA 510(k)-cleared medical device (K221053) manufactured by Fellowship of Orthopaedic Researchers, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 2023. Regulation: 8.