The FDA has given Vertera Spine clearance to market its COALESCE porous PEEK Lumbar Interbody Fusion Device for use in transforaminal, anterior, posterior and lateral lumbar interbody fusion procedures. The device, which comes with the company's porous PEEK biomaterial, will be launched later this year for PLIF and TLIF in different height, footprint and lordotic angle configurations.
FDA clears Vertera Spine's lumbar interbody fusion device
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