Aurora Spine Lands 510(K) Nod From FDA For Spinal Fusion Implants

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Aurora Spine secures 510(k) clearance from the FDA for its TiNano implants for spinal fusion procedures. Aurora Spine (TSX:ASG.V) said it won 510(k) clearance from the FDA for its TiNano coated interbody systems for spinal fusion procedures. Carlsbad, Calif.-based Aurora said the implants are coated with a titanium plasma spraydesigned to encourage bpone ingrowth.

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