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

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

The 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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