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DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914602
510(k) Type
Traditional
Applicant
THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1991
Days to Decision
38 days
Submission Type
Summary

DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914602
510(k) Type
Traditional
Applicant
THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1991
Days to Decision
38 days
Submission Type
Summary