# K241207: SmartClaw™ Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw™ Thrombectomy Catheter, 32 mm (FD0660-02)

- Pathway: 510(k) (Special)
- Applicant: Devoro Medical, Inc.
- Decided: May 29, 2024 after 29 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: 8 generations back to K832023 (1983). 21 ancestors in all.
No later device cites it as a predicate yet.
3 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221391: WOLF Thrombectomy™ SmartClaw Catheter, Devoro Medical, Inc. (2022) Summary page 4.

## Indications for use
The SmartClaw™ Thrombectomy Catheter is indicated for the non-surgical removal of thrombi and emboli from the peripheral vasculature.

Source page: https://510kreport.com/device/K241207
Methodology: https://510kreport.com/methodology