TruLift Lateral Expandable Spacer System & Lateral Plate System

TruLift Lateral Expandable Spacer System & Lateral Plate System is an FDA 510(k)-cleared medical device (K221806) 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 December 4, 2022. Regulation: 8.