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MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972944
510(k) Type
Traditional
Applicant
Medtronics Interventional Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1997
Days to Decision
84 days
Submission Type
Summary

MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972944
510(k) Type
Traditional
Applicant
Medtronics Interventional Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1997
Days to Decision
84 days
Submission Type
Summary