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Medical Devices / Submissions and Approvals

Renovis Gains FDA Clearance for Interbody Spinal Fusion System

July 2, 2018
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Renovis won 510(k) clearance for its Tesera SA hyperlordotic anterior lumbar interbody spinal fusion system.

The porous, titanium implants feature a four-screw design and a locking cover plate to prevent the screws from backing out.

The implants are made using 3D printing, with a porous surface structure that enables in-growth and bone attachment to the implant.

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