TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is an FDA 510(k)-cleared medical device (K251502) manufactured by Life Spine, 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 July 6, 2025. Regulation: 8.