# K972944: Medtronic Mustang Super Floppy Guide Wire/Floppy Guide Wire/Intermediate Guide Wire/Standard Guide Wire/Extra Support

- Pathway: 510(k) (Traditional)
- Applicant: Medtronics Interventional Vascular
- Decided: Nov 3, 1997 after 84 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.
No later device cites it as a predicate yet.
0 of 1 device 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) ACS® Hi-Torque Intermediate® Guide Wire: named in the summary without a submission number
- (no number) ACS® Hi-Torque Standard® Guide Wire: named in the summary without a submission number
- (no number) ACS® Hi-Torque Extra S’port™ 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

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

Source page: https://510kreport.com/device/K972944
Methodology: https://510kreport.com/methodology