# K961917: Medtronic Mustang Steerable Guide Wire (M-45FR, M45FX)

- Pathway: 510(k) (Traditional)
- Applicant: Medtronics Interventional Vascular
- Decided: Nov 20, 1996 after 187 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
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) ACS® Hi Torque Floppy II® Guide Wire: named in the summary without a submission number
- (no number) Scimed® Sceptor™ Floppy Guide Wire: named in the summary without a submission number

## Most influential descendants
- K982272: Galeo HS 014 Model 117 130, Galeo S 014 Model 115 488, Galeao M 014 Model 114156, Galeo F 014 Model 115 487 Galeo HF 018 (1999), 2 descendants of its own
- K090193: Conductor Coronary Guidewire (2009), 0 descendants of its own
- K042373: Galeo Focus Guide Wire (2005), 0 descendants of its own

## Indications for use
The Medtronic® MUSTANG™ Steerable Guide Wire is for use in introducing and placing interventional catheters during percutaneous transiuminal coronary angioplasty (PTCA) and/or percutaneous transluminal angioplasty (PTA).

Source page: https://510kreport.com/device/K961917
Methodology: https://510kreport.com/methodology