Last synced on 30 September 2022 at 11:05 pm

Duatene bilayer mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172395
510(k) Type
Traditional
Applicant
Sofradim Production
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/1/2018
Days to Decision
177 days
Submission Type
Summary

Duatene bilayer mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172395
510(k) Type
Traditional
Applicant
Sofradim Production
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/1/2018
Days to Decision
177 days
Submission Type
Summary