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Camber Spine Gains FDA Clearance for ENZA-A Titanium ALIF -

Camber Spine received FDA 510(k) clearance to market the ENZA™-A Titanium Anterior Lumbar Interbody Fusion system. ENZA™-A comprises a 3D printed body with a roughened surface and 500 micron-sized pores in the upper and lower faces to support bone ingrowth. Multiple openings can accept a large volume of autogenous bone graft. ENZA-A features two sharpened anchor plates inside the body that are deployed into adjacent vertebrae to provide fixation. A single inline instrument inserts, deploys and locks the device in place. (Camber Spine, 6/4/18)