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Accuray seeks US FDA marketing approval for Radixact treatment delivery system
Sunnyvale, California | Thursday, April 28, 2016, 16:00 Hrs  [IST]

Accuray Incorporated, a radiation oncology company, announced the submission of its 510(k) premarket notification with the Food and Drug Administration (FDA) for the company’s Radixact Treatment Delivery System. Accuray also submitted 510(k) premarket notification for its treatment planning and data management systems, Precision Treatment Planning System and iDMS Data Management System.

The treatment delivery system, Precision Treatment Planning System, and iDMS Data Management System have been designed to seamlessly work together and improve treatment workflow processes. Multiple Radixact Systems may use a single, centralized database for treatment planning and patient data management.

“The Radixact System is the next generation TomoTherapy platform and is being designed to leverage its unique architecture, providing a mainstream option for more clinicians. The new platform, comprised of the treatment delivery, treatment planning and data management systems, is expected to expand clinical capabilities while significantly increasing the ease and speed with which clinicians can provide precise radiation treatments,” said Joshua H. Levine, president and chief executive officer of Accuray. “The Radixact System will provide the foundation for continued innovation in the months and years ahead. Working with clinicians we will continue the development of clinically relevant, leading-edge technologies with the potential to truly change the radiation therapy treatment experience.”

The next generation platform is designed for increased throughput, higher reliability and ease of serviceability. The ring gantry-based delivery system will offer the same proven gold-standard delivery capabilities as today’s devices: TomoHelical and TomoDirect treatment modes. The high output, compact linear accelerator will be capable of producing a dose rate of 1,000 MU per minute, and imaging speed will increase. The integrated treatment planning system is intended to reduce workflow complexities and save time in the treatment planning process.

Clinicians at the University of Wisconsin-Madison played an important role in developing this newest radiation therapy system, collaborating with Accuray to ensure the Radixact System design objectives were met.

“The University of Wisconsin team is excited to be involved in the development of a new radiation therapy technology which builds upon the pioneering work initiated here,” said Jennifer Smilowitz, PhD, clinical associate professor University of Wisconsin School of Medicine and Public Health. “We look forward to sharing the initial experiences of our Radixact System work at the ESTRO meeting in Turin, Italy on May 1, 2016.”

The Radixact Treatment Delivery System, Precision Treatment Planning System and iDMS Data Management System are pending FDA 510(k) clearance and not available for sale within the United States. These products may also be subject to international regulatory approval or licensing processes such that the availability of these products may vary according to geographical location.

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