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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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.More Articles on Devices:
5 Recent Orthopedic Device Company Expansions & Agreements
SpineCraft Signs Distribution Agreement With Zimmer
Stryker Q1 Net Earnings Drop 13% After Hip Implant Recalls