KMTI Tesera SA Anterior Lumbar Interbody Fusion (ALIF) System

KMTI Tesera SA Anterior Lumbar Interbody Fusion (ALIF) System is an FDA 510(k)-cleared medical device (K193320) manufactured by Kyocera Medical Technologies, 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 3, 2020. Regulation: 8.