Last synced on 25 January 2026 at 3:41 am

GTX GUIDEWIRE, MODELS TBD-GTX 1, 3,6,9,12, 15

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091582
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2009
Days to Decision
185 days
Submission Type
Summary

GTX GUIDEWIRE, MODELS TBD-GTX 1, 3,6,9,12, 15

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091582
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2009
Days to Decision
185 days
Submission Type
Summary