Carlsbad, Calif.-based Aurora Spine has received FDA 510(k) clearance for TiNano spinal fusion implant.
The TiNano is a sterile-packed, titanium plasma spray-coated device. It's a PEEK interbody implant that promotes bone ingrowth.
TiNano joins Aurora's growing portfolio of FDA-approved devices, including the ZIP Minimally Invasive Interspinous Fusion System.
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TiNano joins Aurora's growing portfolio of FDA-approved devices, including the ZIP Minimally Invasive Interspinous Fusion System.
More Articles on Devices:
Smith & Nephew to Purchase ArthroCare for $1.7B
Global Medical Device Market to Reach $434.4B by 2017
Zimmer Holdings Reports Strong Q4, Year-End Earnings of $761M