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RELIANT STENT GRAFT BALLOON CATHETER

Page Type
Cleared 510(K)
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)
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