Last synced on 25 January 2026 at 3:41 am

Medtronic Stedi Extra Support Guidewire

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250075
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2025
Days to Decision
154 days
Submission Type
Summary

Medtronic Stedi Extra Support Guidewire

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250075
510(k) Type
Traditional
Applicant
Medtronic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2025
Days to Decision
154 days
Submission Type
Summary