Vy Spine®, a spine innovation leader using differentiated materials and designs, announced today that it has received 510(k) clearance from the FDA for its VyBrate™ VBR System which is designed for use in both the cervical and thoracolumbar spine for vertebral body replacement surgery.
The VyBrate™ VBR is an innovative device combining the osseointegration properties of the OXPEKK™ material and the novel OsteoVy™ lattice structure unique to Vy Spine®. Additionally, the VyBrate™ VBR device is the first vertebral body replacement device on the market made using OsteoVy™ #PEKK.
source : Vy Spine
#VySpine #VyBrate #PEKK
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