Life Spine’s ProLift Spinal System Gets FDA’s 510(k) Clearance

Life Spine has received the FDA’s 510(k) clearance for its ProLift micro expandable spacer system, a spinal device.

The ProLift micro, which features a self-locking design that is adjustable to the individual patient’s pathology and anatomy, is available in a range of sizes.

The device is intended for “micro invasive” procedures such as endoscopic transforaminal lumbar interbody fusions, the Huntley, Ill.-based company said.