FDA clears Xoft brachytherapy device

AuntMinnie.com staff writers
Mar 16, 2008

The U.S. Food and Drug Administration (FDA) has cleared new indications for a brachytherapy device from Xoft of Sunnyvale, CA.

The company's Axxent electronic brachytherapy system is designed to be used in minimally shielded environments and to deliver localized, nonradioactive, isotope-free radiation treatment. The product was previously cleared for accelerated treatment of early-stage breast cancer, but is now available for treatment of other cancers in which radiation therapy is indicated, the company reported.

Related Reading

Xoft reports new CPT code, July 26, 2007

Xoft reaches milestone, April 25, 2007

FDA clears Xoft brachytherapy unit, January 5, 2006

Varian, Xoft sign distribution deal, October 13, 2005

Copyright © 2007 AuntMinnie.com

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