InFill Interbody Fusion Devices

InFill Interbody Fusion Devices is an FDA 510(k)-cleared medical device (K150206) manufactured by Pinnacle Spine Group, 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 April 2, 2015. Regulation: 8.