Last synced on 19 July 2024 at 11:05 pm

VitaMESH Macroporous PP Surgical Mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172636
510(k) Type
Traditional
Applicant
Proxy Biomedical Ltd.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/30/2018
Days to Decision
241 days
Submission Type
Summary

VitaMESH Macroporous PP Surgical Mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172636
510(k) Type
Traditional
Applicant
Proxy Biomedical Ltd.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/30/2018
Days to Decision
241 days
Submission Type
Summary