# K232730: Aventus Thrombectomy System

- Pathway: 510(k) (Traditional)
- Applicant: Inquis Medical
- Decided: Nov 1, 2023 after 55 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: 6 generations back to K183198 (2018). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K223929: Laguna™ Clot Retriever System and Malibu™ Aspiration Catheter System (Laguna Thrombectomy System), Innova Vascular, Inc. (2023) Summary page 4.

## 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/K232730
Methodology: https://510kreport.com/methodology