Renovis Surgical received FDA clearance for its Tesera Standalone anterior lumbar interbody fusion cage.
The Tesera is a porous titanium spinal implant — one of the first such devices with a true porous structure — for long term stability and fusion. The cage is crafted through melting titanium alloy powder with an electric beam.
Renovis will launch other titanium porous devices later this year.
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The Tesera is a porous titanium spinal implant — one of the first such devices with a true porous structure — for long term stability and fusion. The cage is crafted through melting titanium alloy powder with an electric beam.
Renovis will launch other titanium porous devices later this year.
More Articles on Supply Chain:
Johnson & Johnson to Dole Out $4B in Metal Hip Replacement Lawsuit Settlement
Device Companies — 7 Key Notes — Biomet, MAKO Surgical & More
Victrex Group Finance Director Steve Barrow to Step Down