Lateral Spine Truss System (LSTS) Interbody Fusion Device

Lateral Spine Truss System (LSTS) Interbody Fusion Device is an FDA 510(k)-cleared medical device (K211388) manufactured by 4Web Medical, 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 August 4, 2021. Regulation: 8.