Life Spine receives FDA approval for Prolift interbody fusion implant

Patsy Newitt -   Print  |

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

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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