Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced that it has received a 510(k) clearance from the US Food and 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, senior 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.
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