FDAnews Device Daily Bulletin
Medical Devices / Submissions and Approvals

Renovis Gains FDA Clearance for Interbody Spinal Fusion System

July 2, 2018

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.

View today's stories