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Exogenesis Hernia Mesh

Page Type
Cleared 510(K)
510(k) Number
K191545
510(k) Type
Traditional
Applicant
Exogenesis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2019
Days to Decision
107 days
Submission Type
Summary

Exogenesis Hernia Mesh

Page Type
Cleared 510(K)
510(k) Number
K191545
510(k) Type
Traditional
Applicant
Exogenesis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2019
Days to Decision
107 days
Submission Type
Summary