Last synced on 19 July 2024 at 11:05 pm

Parietex Surgical Mesh (modified into Parietex Hydrophilic 2D, 3D, Anatomical Mesh), Parietex Composite Mesh (PCO and PCO-OS references), Parietex Optimized Composite Mesh (PCO-X, PCO-FX and PCO-OSX references)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173796
510(k) Type
Traditional
Applicant
Sofradim Production
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/9/2018
Days to Decision
85 days
Submission Type
Summary

Parietex Surgical Mesh (modified into Parietex Hydrophilic 2D, 3D, Anatomical Mesh), Parietex Composite Mesh (PCO and PCO-OS references), Parietex Optimized Composite Mesh (PCO-X, PCO-FX and PCO-OSX references)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173796
510(k) Type
Traditional
Applicant
Sofradim Production
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/9/2018
Days to Decision
85 days
Submission Type
Summary