Stereotaxis Receives FDA 510(k) Clearance for Synchrony System
Stereotaxis announced that it has received FDA 510(k) clearance 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 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."
