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Medtronic Mustang Super Floppy Guide Wire/Floppy Guide Wire/Intermediate Guide Wire/Standard Guide Wire/Extra Support

by Medtronics Interventional Vascular

510(k) K972944

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK972944 Date3 Nov 1997ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DQX
Device Class
Class II
Regulation
21 CFR Part 870.1330
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 24 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Medtronic Mustang Steerable Guide Wire is a 0.014 inch diameter guidewire designed to facilitate the introduction and placement of interventional catheters within the vasculature. It features a polymer-coated proximal shaft, a lubricious distal coating, and a radiopaque spring tip to assist with visualization under fluoroscopy.

This device is used by physicians during PTCA or PTA procedures. It is identified under FDA 510k number K972944.

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