FDA clears new minimally invasive Life Spine device

Spinal Tech

Life Spine received FDA 510(k) clearance for its new Prolift Lateral Expandable Spacer System.

Prolift features minimal insertion height and controlled in-situ expansion which are key in a minimally invasive expandable lateral interbody fusion.

The device will be available in several footprint and lordotic options.

"The Prolift Lateral Expandable Spacer System is a significant addition to Life Spine’s rapidly growing expandable portfolio," said Rich Mueller, COO of Life Spine. "The device… has anatomically convex endplates and has Life Spine's proprietary OSSEO-LOC surface technology."

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