# K120137: Victory Guidewire (32 Models)

- Pathway: 510(k) (Special)
- Applicant: Brivant, Ltd.
- Decided: Feb 14, 2012 after 28 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: 7 generations back to K970376 (1997). 15 ancestors in all.
No later device cites it as a predicate yet.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102211: Cruiser 18 Guidewire, Brivant, Ltd. (2010) Summary page 1.

## Indications for use
The guidewires are intended to facilitate the placement and exchange of balloon catheters or other interventional devices within the peripheral vasculature during Percutaneous Transluminal Angioplasty (PTA) or other intravascular interventional procedures.

Source page: https://510kreport.com/device/K120137
Methodology: https://510kreport.com/methodology