The ClearPoint 2.0 software, which received 510(k) clearance in 2018, recently obtained CE mark and is now available to our European customers. The software utilizes a hospital’s existing diagnostic-only or intraoperative MRI suite, and works to enable a range of minimally invasive procedures in the brain.
ClearPoint 2.0 Software Approved for Use In Europe
One of the main goals of the ClearPoint 2.0 project was to re-develop the software using a new visualization platform while improving functionality and ensuring compatibility with Windows 10. ClearPoint 2.0 optimizes existing workflows for more efficient clinical interaction with new feature sets including: image fusion, volume of interest (VOI) enhanced 3D viewing, multi-trajectory planning as well as an optimized user experience of the Navigation System.
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