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.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1m3tXwt
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