Spinal Tech

Amedica Receives FDA Approval for Interbody Fusion Device

Amedica, a spinal and reconstructive medical device manufacturer, has received 510(k) clearance from the FDA to legally market a second generation family of cervical and lumbar interbody fusion devices manufactured with the company’s proprietary silicon nitride biomaterial.

Jaimie Oh

Thursday, September 27th, 2012

The product portfolio expansion offers design enhancements including a threaded insertion feature, additional footprints and design elements that will allow surgeons to perform minimally invasive and lumbar lateral interbody fusion approaches.

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