ProLift Micro Expandable Spacer System

ProLift Micro Expandable Spacer System is an FDA 510(k)-cleared medical device (K223430) 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 May 3, 2023. Regulation: 8.