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PARIETEX OPTIMIZED COMPOSTIE MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110815
510(k) Type
Special
Applicant
SOFRADIM PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2011
Days to Decision
26 days
Submission Type
Summary

PARIETEX OPTIMIZED COMPOSTIE MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110815
510(k) Type
Special
Applicant
SOFRADIM PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2011
Days to Decision
26 days
Submission Type
Summary