Matrix HA Fusion Porous Cervical IBF System

Matrix HA Fusion Porous Cervical IBF System is an FDA 510(k)-cleared medical device (K223510) manufactured by Innovasis, 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 December 11, 2022. Regulation: 8.