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

free biotech news Get the latest biotech news where you want it. Sign up for the free GenePool newsletter today!

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.

Help employers find you! Check out all the jobs and post your resume.

Back to news