LIBERTY Endovascular Robotic System Context

Specifications

Setup Time Min: Under 5 min
Radiation Exposure Reduction: 92% reduction reported in cited clinical evidence
Instrument Compatibility: Commercially available guidewires, catheters, and guide catheters within cleared specifications
Regulatory Clearance: FDA 510(k) cleared for peripheral endovascular procedures
Regulatory Status: FDA 510(k) cleared on 8 September 2025
Use Model: Single-use remotely operated endovascular robotic system
Intended Use: Remote delivery and manipulation of guidewires and catheters, and remote manipulation of guide catheters, in the peripheral vasculature
Scope Limit: Not intended for coronary or neurointerventional procedures