# K240117: Aventus Thrombectomy System (IM-2001/IM-0002)

- Pathway: 510(k) (Traditional)
- Applicant: Inquis Medical
- Decided: Mar 15, 2024 after 59 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
No predicates in its family tree.
2 later devices descend 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)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K191968: Aventus Thrombectomy System. Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Most influential descendants
- K250202: Aventus Thrombectomy System (2025), 1 descendant of its own
- 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/K240117
Methodology: https://510kreport.com/methodology