InFill Interbody Fusion Device

InFill Interbody Fusion Device is an FDA 510(k)-cleared medical device (K152259) 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 November 18, 2015. Regulation: 8.