Life Spine Gains FDA 510(k) for the PLATEAU-X Ti Lateral Lumbar Spacer

By Julie A. Vetalice

Life Spine Gains FDA 510(k) for the PLATEAU-X Ti Lateral Lumbar Spacer

Life Spine received FDA 510(k) clearance to market the PLATEAU®-X Ti Lateral Lumbar Spacer System.

The system comprises instruments and implants to streamline the surgical procedure. Features include:

  • Self-distracting leading edge to ease implant insertion
  • Osseo-Loc™ Titanium Surface Treatment Technology
  • Convex design maximizes vertebrae endplate contact for ideal patient fit
  • Large, open graft windows for maximum visibility and bone graft containment

“The launch of PLATEAU-X Ti furthers our commitment of offering micro invasive solutions that are designed to save time, save money, and accelerate patient recovery,” said Mariusz Knap, Senior Vice President of Sales and Marketing. “PLATEAU-X Ti and all of our titanium implants offer a proprietary surface treatment, Osseo-Loc™. PLATEAU-X Ti improves our already extensive lateral portfolio comprised of PROLIFT® Lateral Expandable Spacer System, CENTRIC® Plier-Style Retractor, and SENTRY® Lateral Plating Systems.”

Product Labels: Lumbar Spine, Spinal Fusion

Tags: 510(k) Clearance, Regulatory