Lateral Spinal Truss System (LSTS) Interbody Fusion Device

Lateral Spinal Truss System (LSTS) Interbody Fusion Device is an FDA 510(k)-cleared medical device (K172392) manufactured by 4Web, 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 November 6, 2017. Regulation: 8.