WAYNE, Pa., May 5, 2016 – Camber Spine Technologies announces  that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its ENZA™ Zero Profile Anterior Interbody Fusion (ALIF) system, a unique, minimally invasive interbody fusion device providing integrated fixation.  This clearance marks Camber’s eighth line of spinal implant systems […]