# K243789: LIBERTY Endovascular Robotic System (LIBERTYOS)

- Pathway: 510(k) (Traditional)
- Applicant: Microbot Medical, Ltd.
- Decided: Sep 4, 2025 after 269 days
- Product code: DXX (System, Catheter Control, Steerable)
- Device class: 2
- Regulation: 21 CFR 870.1290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K900765 (1990). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151730: Magellan Robotic System, Hansen Medical, Inc. (2015) Summary page 5.

## Indications for use
The LIBERTY® Endovascular Robotic System is intended for use in the remote delivery and manipulation of guidewires and catheters, and remote manipulation of guide catheters, to facilitate navigation to anatomical targets in the peripheral vasculature. The LIBERTY® Endovascular Robotic System is not intended for coronary or neurointerventional procedures.

Source page: https://510kreport.com/device/K243789
Methodology: https://510kreport.com/methodology