FDA Grants 510(k) Approval to Accuray Data Management System

August 3, 2017

Accuray has secured 510(k) clearance from the FDA for its iDMS data management system.

The system will be used to integrate data from Accuray’s technology platforms such as the TomoTherapy and CyberKnife systems. It allows users to store and manage patient data across numerous devices.

The approval comes shortly after the company published data showing a higher patient survival rate for its TomoTherapy radiation therapy system compared to Varian Medical’s RapidArc radiotherapy system.

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