Last synced on 23 September 2022 at 11:05 pm

GORE SYNECOR Preperitoneal Biomaterial

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163576
510(k) Type
Traditional
Applicant
W. L. Gore & Associates, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
143 days
Submission Type
Summary

GORE SYNECOR Preperitoneal Biomaterial

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163576
510(k) Type
Traditional
Applicant
W. L. Gore & Associates, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
143 days
Submission Type
Summary