Life Spine Gains Additional FDA 510(k) Clearance for PROLIFT Expandable Spacer

By Julie A. Vetalice

Life Spine received an additional FDA 510(k) clearance to market additional sizes of the PROLIFT® Expandable Spacer System. This addition more than doubles PROLIFT's current footprint options.

The new 8mm to 10mm widths are designed to decrease patient trauma through smaller incisions and less retraction. Like other devices in the PROLIFT line, they can be post-packed in situ and feature OSSEO-LOC™ surface technology with 400 to 600 microns of porosity to support bone on-growth.

Source: Life Spine

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory