Ancora LLC Interbody Fusion Device

Ancora LLC Interbody Fusion Device is an FDA 510(k)-cleared medical device (K143228) manufactured by Frontier Medical Devices, 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 25, 2015. Regulation: 8.