# K063371: Pronto V3 Extraction Catheter, Model 5003

- Pathway: 510(k) (Traditional)
- Applicant: Vascular Solutions, Inc.
- Decided: Dec 14, 2006 after 36 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- 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 K052232 (2005). 1 ancestor in all.
27 later devices descend from it; 8 cite it directly.
1 of 29 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052232: Vascular Solutions Pronto V3 Extraction Catheter, Vascular Solutions, Inc. (2005) Summary page 5.

## Most influential descendants
- K071727: QXT Extraction Catheter (2007), 12 descendants of its own
- K072810: Pronto Low Profile (LP) Extraction Catheter, Model 5010 (2007), 11 descendants of its own
- K083784: Pronto V3 Extraction Center, Model 5003, Pronto LP Extraction Catheter, Model 5010, Skyway RX Support Catheter, (2009), 10 descendants of its own
- K113757: Aspire Max Aspiration Catheter (2012), 5 descendants of its own
- K103405: Pronto V4 Extraction Catheter 5.5F; Pronto V4 Extraction Catheter 6F; Pronto V4 Extraction 7F; Pronto V4 Extraction Cath (2010), 4 descendants of its own

## Indications for use
The Pronto catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K063371
Methodology: https://510kreport.com/methodology