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RESTORELLE POLYPROPYLENE MESH; RESTORELLE POLYPROPYLENE MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103568
510(k) Type
Special
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2010
Days to Decision
16 days
Submission Type
Summary

RESTORELLE POLYPROPYLENE MESH; RESTORELLE POLYPROPYLENE MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103568
510(k) Type
Special
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2010
Days to Decision
16 days
Submission Type
Summary