Elekta Unity, world’s first high field MR-linac, receives FDA 510(k) clearance
New radiation therapy system will now be implemented clinically in U.S., ushering in a transformation in precision and personalized cancer treatmentSTOCKHOLM, December 5, 2018 – Elekta (EKTA-B.ST) today announced that its Elekta Unity magnetic resonance radiation therapy (MR/RT) system has received 510(k) premarket notification from the U.S. Food and Drug Administration, clearing the technology for commercial sales and clinical use in the United States. “Since receiving CE mark in June 2018, Elekta Unity has been transforming the care of cancer patients in Europe, and we are excited that