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RESTORELLE POLYPROPYLENE MESH

Page Type
Cleared 510(K)
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)
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