Talos-C(HA) Cervical Intervertebral Body Fusion Devices

Talos-C(HA) Cervical Intervertebral Body Fusion Devices is an FDA 510(k)-cleared medical device (K142345) manufactured by Meditech Spine, 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 February 21, 2015. Regulation: 8.