# K200871: Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator

- Pathway: 510(k) (Special)
- Applicant: Control Medical Technology
- Decided: May 4, 2020 after 33 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: 9 generations back to K904788 (1990). 73 ancestors in all.
1 later device descends from it; 1 cites it directly.
3 of 75 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113757: Aspire Max Aspiration Catheter, Control Medical Technology, LLC (2012) Summary page 4.

## Most influential descendants
- 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

## Indications for use
The Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator is indicated for the removal of fresh soft emboli and thrombi from vessels in the peripheral vasculature.

Source page: https://510kreport.com/device/K200871
Methodology: https://510kreport.com/methodology