Life Spine Gains FDA Clearance for PROLIFT Lateral Expandable Spacer

By Julie A. Vetalice

Life Spine received FDA 510(k) clearance to market the PROLIFT® Lateral Expandable Spacer system.

PROLIFT Lateral features minimal insertion height and controlled, in situ expansion, and is complemented by the company's full lateral portfolio: the CENTRIC® Retractor, Lateral Disc Prep, OSTEO-LINE® Graft Delivery device, neuromonitoring instruments, LONGBOW®Expandable Spacer and SENTRY® Lateral Plating.

Source: Life Spine

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory