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RESTORELLE POLYPROPYLENE MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092207
510(k) Type
Special
Applicant
MPATHY MEDICAL DEVICES INC
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/4/2009
Days to Decision
13 days
Submission Type
Summary

RESTORELLE POLYPROPYLENE MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092207
510(k) Type
Special
Applicant
MPATHY MEDICAL DEVICES INC
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/4/2009
Days to Decision
13 days
Submission Type
Summary