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# Microbot Single-Use Robotic Endovascular System Cleared
- URL: https://www.fdaweb.com/microbot-single-use-robotic-endovascular-system-cleared/
- Published: 2025-09-09T12:00:00.000Z
- Updated: 2026-09-14T15:21:12.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5159838

FDA has cleared a Microbot Medical 510(k) for its Liberty Endovascular Robotic System, a single-use, remotely operated device designed for peripheral endovascular procedures. The pivotal trial supporting clearance demonstrated 100% success in robotic navigation to the target with no device-related adverse events, as well as a 92% relative reduction in physician radiation exposure, the company says. Its remote design is also expected to improve ergonomics and reduce physical strain on providers, it adds.