Last synced on 14 November 2025 at 11:06 pm

Medtronic Stedi Extra Support Guidewire

Page Type
Cleared 510(K)
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)
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