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Stereotaxis announces EU launch, 510k submission for Synchrony system

Stereotaxis (STXS) announced it obtained CE Mark in Europe and submitted a 510(k) application to the FDA in the US for the Synchrony system. “Synchrony and SynX are central to our digital surgery efforts to modernize the interventional lab with enhanced workflow, remote connectivity, and smart AI capabilities,” said David Fischel, Stereotaxis Chairman and CEO. “The technology improves the robotic cockpit, and will be critical in supporting future robotic efforts for remote long-distance procedures and automated catheter navigation. The opportunity is much broader than robotic labs as we believe all cath labs stand to benefit from improved workflow, connectivity, and collaboration.”

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