Amedica Receives FDA 510(k) Clearance For A Second Generation Interbody Fusion Device System

Amedica Corporation, a spinal and reconstructive medical device manufacturer, announced today it has received FDA 510(k) clearance to legally market a second generation family of cervical and lumbar interbody fusion devices manufactured with the company’s proprietary Silicon Nitride biomaterial. The product offers design enhancements the company says will allow surgeons to perform minimally invasive and lumbar lateral interbody fusion approaches.