# K220716: Spartan SC 069

- Pathway: 510(k) (Traditional)
- Applicant: Spartan Micro, Inc.
- Decided: May 5, 2022 after 55 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K003880 (2001). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180715: React 68 Catheter, Micro Therapeutics, Inc. d/b/a ev3 Neurovascular (2018) Summary page 4.

## Indications for use
The Spartan SC 069™ is indicated for the introduction of interventional devices into the peripheral and neuro vasculature.

Source page: https://510kreport.com/device/K220716
Methodology: https://510kreport.com/methodology