Renovis wins FDA nod for Tesera ALIF interbody spinal fusion system

Renovis Surgical Technologies said today that it won 510(k) clearance from the FDA for its Tesera SA hyperlordotic ALIF interbody spinal fusion system.

The company’s porous, titanium, stand-alone anterior lumbar interbody fusion system features a four-screw design and a locking cover plate designed to prevent screw backout.

Renovis’ Tesera implants are made using additive manufacturing, according to the company, and include a porous surface structure to enable bone attachment and in-growth to the implant.

With its latest regulatory win, Renovis’ portfolio of 3D-printed titanium implant systems include anterior cervical, anterior lumbar and posterior lumbar devices.

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