Another FDA 510(k) clearance for Synaptive Medical with its ImageDrive Pro

by Fink Densford for

Synaptive Medical said it won FDA 510(k) clearance for its ImageDrive Pro informatics system designed to integrate its existing BrightMatter technology into multiple platforms.

The company said the new platform will allow for interoperability across all of BrightMatter’s solutions, including imaging, surgical planning, navigation and automated positioning of high definition optics.

BrightMatter gives 3D visuals of the brain in the operating room, which help guide surgeons as they pursue neurological procedures. During surgery, the images are placed over an anatomical scan, offering a way to visualize the inside of the brain.

“The need for deeper interconnectivity and integration of our own systems and data platforms is essential as we look at introducing novel imaging and sensing technologies in the near future. Our platform is uniquely designed to provide transformative data insights and make an impact in the continuum of care for patients undergoing various surgical treatments,” prez Cameron Piron said in a press release.

Toronto-based Synaptive Medical said its platform will allow for a more “unified experience” for interdisciplinary review through automated data distribution, de-identification and extensability using well-established protocols.

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