Life Spine Earns 510(k) Clearance for Lateral Expandable System

The FDA granted Life Spine 510(k) clearance for its PROLIFT lateral expandable spacer system, a device that helps to restore patient disc height and aids in spinal decompression.

The device has a small starting size and is designed to minimize impaction and preserve the integrity of the vertebral end plate.

The micro-invasive device uses a bulleted tip to simplify insertion and can be collapsed or expanded following placement.