Last synced on 30 May 2025 at 11:05 pm

Duravess bovine pericardial vascular patch

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172660
510(k) Type
Traditional
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2017
Days to Decision
73 days
Submission Type
Summary

Duravess bovine pericardial vascular patch

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172660
510(k) Type
Traditional
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2017
Days to Decision
73 days
Submission Type
Summary