Life Spine Announces FDA 510(k) Clearance for the PROLIFT Wedge Expandable Spacer System

By Julie A. Vetalice

Life Spine Announces FDA 510(k) Clearance for the PROLIFT Wedge Expandable Spacer System

Life Spine was granted FDA 510(k) clearance to market the PROLIFT® Wedge Expandable Spacer System.

The system, featuring OSSEO-LOC™ Surface Technology, is a lordotic expandable implant for Micro Invasive TLIF and PLIF.  The implant is designed with multiple implant heights and widths to optimally fit the patient’s disc anatomy. Once the patient specific correction has been achieved, PROLIFT Wedge is auto-locked in position and can be packed with graft in situ through the OSTEO-LINE™ Graft Delivery Device.

The PROLIFT Wedge Expandable Spacer marks the company’s 11th expandable 510(k) clearance that includes expandable solutions for PLIF, TLIF and LATERAL procedures.

“The launch of PROLIFT Wedge furthers our commitment to offering patient matched expandable solutions,” said Mariusz Knap, Senior Vice President of Sales and Marketing for Life Spine. “PROLIFT Wedge is another innovative expandable interbody added to our existing portfolio providing surgeons with multiple solutions for improving patient care.”

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory