Last synced on 19 July 2024 at 11:05 pm

PARIETEX COMPOSITE MONO PM MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081126
510(k) Type
Traditional
Applicant
SOFRADIM PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2008
Days to Decision
114 days
Submission Type
Summary

PARIETEX COMPOSITE MONO PM MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081126
510(k) Type
Traditional
Applicant
SOFRADIM PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2008
Days to Decision
114 days
Submission Type
Summary