Camber Spine Technologies announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its SPIRA™ Open Matrix ALIF device, a interbody fusion implant consisting of spiral support arches and Surface by Design™ technology. This clearance marks Camber’s tenth line of spinal implant systems to be released in the US market. Continue reading “AM implants by Camber Spine Technologies receive FDA clearance”
AM implants by Camber Spine Technologies receive FDA clearance
