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Reimbursement / Regulatory

Renovis Surgical Gains FDA Clearance for New Tesera ALIF System -

Renovis Surgical Technologies received FDA 510(k) clearance to market Tesera® SA Hyperlordotic ALIF, a standalone interbody fusion system. Like the rest of the company's Tesera implants, SA-HL is made using additive manufacturing to create a roughened, highly porous surface to support bone attachment and ingrowth. A four-screw design and locking cover plate are intended to prevent screw backout. (Renovis Surgical Technologies, 6/28/18)