NGMedical Gains FDA 510(k) for AM Titanium Lumbar Interbody BEE PLIF

By Julie A. Vetalice

NGMedical Gains FDA 510(k) for AM Titanium Lumbar Interbody BEE PLIF

NGMedical received FDA clearance for its purely additively manufactured titanium lumbar BEE® PLIF cage.

The BEE PLIF cage was created to benefit from additive manufacturing features. The purposefully designed honeycomb endplate design reduces the risk of subsidence, while allowing fusion. The honeycomb structure allows for bony ingrowth while offering a very large graft space. Smooth lateral surfaces facilitate insert and rotate technique. BEE PLIF is offered in a wide range of sizes up to 18° lordosis.

Source: NGMedical

 

Product Labels: Lumbar Spine, Spinal Fusion

Tags: 510(k) Clearance, Regulatory