Home » Life Spine Earns 510(k) Clearance for Lateral Expandable System
Life Spine Earns 510(k) Clearance for Lateral Expandable System
March 4, 2020
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.
Upcoming Events
-
21Oct