FDA Grants 510(k) Clearance to Integra LifeSciences’ Hollywood Interbody Device

Plainsboro, N.J.-based Integra LifeSciences Holdings received U.S. FDA 510(k) clearance for its Integra Hollywood NanoMetalene Interbody Device.

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The company will begin a controlled market release later this year. The device is designed to treat transforaminal lumbar interbody fusion.

The Hollywood NanoMetalene is made of PEEK-OPTIMA polymer from Invibio Biomaterials.

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