Aurora Spine Receives FDA 510(k) Approval for TiNano Spinal Fusion Device

Carlsbad, Calif.-based Aurora Spine has received FDA 510(k) clearance for TiNano spinal fusion implant.

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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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