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MINIMAX (TM) HARDSHELL VENOUS RES W/INTE CARD FILT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911789
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1991
Days to Decision
120 days
Submission Type
Statement

MINIMAX (TM) HARDSHELL VENOUS RES W/INTE CARD FILT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911789
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1991
Days to Decision
120 days
Submission Type
Statement