August 28, 2008 – TomoTherapy reported that the FDA has granted 510(k) clearance for its radiation therapy technology, TomoDirect, designed to complement helical tomotherapy and faster treatment planning.
Tomotherapy will unveil TomoDirect at the European Society for Therapeutic radiology and Oncology (ESTRO) in Gothenburg, Sweden, Sept. 14-18, 2008, and the American Society for Therapeutic radiology and Oncology (ASTRO) in Boston, MA, Sept. 21-25, 2008.