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



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

SALT LAKE CITY, Sept. 27, 2012 /PRNewswire/ — Amedica Corporation, a spinal and reconstructive medical device manufacturer, announced today it has received 510(k) clearance from the U.S. Food and Drug Administration to legally market a second generation family of cervical and lumbar interbody fusion…