SHELTON, Conn.--(BUSINESS WIRE)--May 4, 2006--Spine Wave announced today that the Company received FDA 510(k) clearance to market the StaXx(TM) XD Expandable Device. The innovative expandable PEEK spacer, indicated for use as a Vertebral Body Replacement device, will be the first commercial product that the Company will release into the U.S. market.
