# K250202: Aventus Thrombectomy System

- Pathway: 510(k) (Special)
- Applicant: Inquis Medical
- Decided: Feb 26, 2025 after 33 days
- Product code: QEW (Peripheral Mechanical Thrombectomy With Aspiration)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K240117 (2024). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240117: Aventus Thrombectomy System (IM-2001/IM-0002), Inquis Medical (2024) Summary page 5.

## Most influential descendants
- K250668: Aventus Thrombectomy System (IM-2100) (2025), 0 descendants of its own

## Indications for use
The Aventus Thrombectomy System is indicated for: * The non-surgical removal of emboli and thrombi from blood vessels. * Injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel. The Aventus Thrombectomy System is intended for use in the peripheral vasculature.

Source page: https://510kreport.com/device/K250202
Methodology: https://510kreport.com/methodology