Submitted by kBLASTER Team on
by Fink Densford for Massdevice.com
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.
Leverage kBLASTER's result management features of sorting, My Favorites, Saved Search and Search History to find a primary predicate, multiple predicates or reference devices. Build a 510(k) clearance strategy by enabling self-service extraction of actionable insight from more than 63,000 FDA medical device 510(k) clearance summaries, plus more than 76,000 splash pages, for a total of nearly 140,000 records.