# K242557: ClotTriever XL Catheter (41-102)

- Pathway: 510(k) (Special)
- Applicant: Inari Medical, Inc.
- Decided: Sep 27, 2024 after 30 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: 18 generations back to K901627 (1990). 27 ancestors in all.
No later device cites it as a predicate yet.
1 of 28 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K223210: ClotTriever XL Catheter, Inari Medical, Inc. (2023) Summary page 5.

## Indications for use
The ClotTriever Thrombectomy System is indicated for: • The non-surgical removal of thrombi and emboli from blood vessels. • Injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel. The ClotTriever Thrombectomy System is intended for use in the peripheral vasculature including deep vein thrombosis (DVT).

Source page: https://510kreport.com/device/K242557
Methodology: https://510kreport.com/methodology