Renovis Receives FDA Clearance for 3D-Printed PLIF Systems

Renovis Surgical received FDA 510(k) clearance to market Tesera® porous titanium posterior lumbar interbody fusion systems.

All Tesera implants are made using additive manufacturing techniques and Tesera Trabecular Technology®, yielding a highly porous structure to support bone attachment.

This is Renovis' fifth product group featuring...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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