# K220075: Spartan Center Wire

- Pathway: 510(k) (Traditional)
- Applicant: Spartan Micro, Inc.
- Decided: Apr 19, 2022 after 99 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K950113 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022357: Transend 300 ES Guidewire, Model 46-814 & Transend 300 Floppy Guidewire, Model 46-815, Boston Scientific, Target (2002) Summary page 4.

## Indications for use
The Spartan Center Wire™ is indicated for general intravascular use in the peripheral vasculature. It can be deployed into the vessel to facilitate the selective placement of diagnostic or therapeutic catheters. The device is not intended for use in the coronary or neuro vasculature.

Source page: https://510kreport.com/device/K220075
Methodology: https://510kreport.com/methodology