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RELIANT STENT GRAFT BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050038
510(k) Type
Traditional
Applicant
Medtronic Endovascular Innovations
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2005
Days to Decision
96 days
Submission Type
Summary

RELIANT STENT GRAFT BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050038
510(k) Type
Traditional
Applicant
Medtronic Endovascular Innovations
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2005
Days to Decision
96 days
Submission Type
Summary