# K113757: Aspire Max Aspiration Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Control Medical Technology, LLC
- Decided: Feb 22, 2012 after 63 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: 8 generations back to K904788 (1990). 72 ancestors in all.
5 later devices descend from it; 3 cite it directly.
3 of 78 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061958: Medtronic Export XT Catheter, Medtronic Vascular (2006)
- K051193: Vascular Solutions Pronto Short Extraction Catheter, Vascular Solutions, Inc. (2005) Summary page 5.
- K063371: Pronto V3 Extraction Catheter, Model 5003, Vascular Solutions, Inc. (2006) Summary page 5.
- K071529: Xtract Catheter System, Lumen Biomedical, Inc. (2007)
- K080901: Lbi Embolectomy System, Lumen Biomedical, Inc. (2008)

## Most influential descendants
- K220780: ROVO Mechanical Thrombectomy Device (2023), 1 descendant of its own
- K200871: Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator (2020), 1 descendant of its own
- K253730: RoVo Mechanical Thrombectomy System (2026), 0 descendants of its own
- K250013: VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S, VS8-MP90S, VS8-MP100B, VS10-MP100B, VS11-MP60S, VS11-MP90S, VS12-MP100B, 7F-MP60S, 7F-MP90S, 8F-MP60S, 8F-MP100B, 10F-MP100B, 11F-MP60S, 11F-MP90S, 11P-MP60S, 11P-MP90S, 12F-MP100B, V30-ASP) (2025), 0 descendants of its own
- K200629: Aspire Mechanical Aspirator G (2020), 0 descendants of its own

## Indications for use
The Aspire MAX 5 and MAX 6 Aspiration Catheters and Aspirator are indicated for the removal of fresh, soft emboli and thrombi from vessels in the peripheral vasculature.

Source page: https://510kreport.com/device/K113757
Methodology: https://510kreport.com/methodology