Life Spine receives FDA approval for Prolift interbody fusion implant

Life Spine has received 510(k) clearance from the FDA to market its Prolift Wedge Expandable Spacer System.

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The lordotic expandable implant is designed with multiple heights and widths to fit the patient’s disc anatomy during micro-invasive transforaminal lumbar interbody fusion and posterior lumbar interbody fusion procedures, according to a March 17 press release.

The Prolift wedge expandable spacer system will be Life Spine’s 11th 510(k) clearance in expandable solutions for PLIF, TLIF and lateral lumbar interbody fusion procedures.

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