Targeted Strategies for Today's Evolving Markets

MissionIR Blog

Accuray, Inc. (ARAY) Gets FDA Clearance to Market Unique Lung Cancer Treatment

Accuray Inc., a global leader in radiosurgery, focused on non-surgical treatment options for those diagnosed with cancer, today announced that the U.S. Food and Drug Administration (FDA) has granted the company 510(k) clearance to market Lung Optimized Treatment, a new component of the company’s CyberKnife® System.

The CyberKnife system is designed to assist physicians in delivering radiosurgery treatments to patients with lung cancer. To date, the system has been used to treat more than 100,000 patients worldwide.

Lung Optimized Treatment is a non-invasive option to safely treat lung tumors, regardless of tumor location, even those close to such critical structures. Treating tumors in near proximity to vital anatomical structures can be difficult, but Accuray’s technology offers multiple and reduced-risk treatment options.

“Lung Optimized Treatment is a new tool we developed to meet the clinical demand for more flexibility in treating lung cancer patients with radiosurgery and the desire to move away from reliance on fiducial markers,” Chris A. Raanes, senior vice president and chief operating officer for Accuray stated in the press release. “This new technology enables treatments throughout the lung without a single incision, all while safeguarding healthy tissue and structures around the tumor to ensure they are not damaged by radiation.”

Accuray’s CyberKnife Robotic Radiosurgery System is a one-of-its-kind system that uses continual image guidance technology and computer controlled robotic mobility to track, detect and correct tumor and patient movement in real-time throughout the treatment. This enables the delivery of high-dose radiation with ultimate precision, minimizing damage to surrounding healthy tissue, and eliminating the need for head or body stabilization.

The company highlights the importance of innovative technologies in this area of cancer treatement.

“With the FDA 510(k) clearance of Lung Optimized Treatment, we’ve taken the CyberKnife technology to new heights and enabled care for an expanded group of patients,” Euan S. Thomson, Ph.D., president and CEO of Accuray stated. “This is yet another step in our efforts to ensure physicians have access to the treatment choices necessary for their patient, based on the patient’s specific needs. To this end, Accuray continues to investigate ways to improve patient care across various indications.”

For more information visit www.accuray.com

Let us hear your thoughts below:

This entry was posted in Small Cap News. Bookmark the permalink.

Leave a Reply

Your email address will not be published. Required fields are marked *