HUNTLEY, Ill.--(BUSINESS WIRE)--Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market the PLATEAU-X Ti Lateral Lumbar Spacer System.
“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, Sr. Vice President of Sales and Marketing for Life Spine. “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.”
The PLATEAU-X Ti Lateral Lumbar Spacer enables surgeons to effectively provide anterior column support through a lateral approach. The PLATEAU-X Ti Lateral Lumbar Spacer incorporates a comprehensive set of instruments and implants to streamline the surgical procedure.
Key Features and Benefits:
• Self-distracting leading edge to ease implant insertion
• Osseo-Loc™ Titanium Surface Treatment Technology
• Available in 0˚, 7˚ and 15˚ lordosis: 40, 45, 50, 55 and 60mm lengths: 8 - 16mm heights: 18, 22 and 26mm widths
• Convex design maximizes vertebrae endplate contact for ideal patient fit
• Large, open graft windows for maximum visibility and bone graft containment
About Life Spine
Life Spine is dedicated to improving the quality of life for spinal patients by increasing procedural efficiency and efficacy through innovative design, uncompromising quality standards, and the most technologically advanced manufacturing platforms. Life Spine, which is privately held, is based in Huntley, Illinois. For more information, please visit: http://www.lifespine.com and/or https://www.micro-invasive.com.
