Spine Wave Intervertebral Body Fusion Device Receives FDA 510(k) Clearance

Shelton, Conn.-based Spine Wave received FDA 510(k) clearance for its StaXx IB System, an intervertebral body fusion device.

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Spine Wave receives FDA 510(k) clearanceThe device combines PEEK spacer technology with bone graft chambers. The StaXx system will be previewed at the American Academy of Neurosurgeons annual meeting in New Orleans.

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