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ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug

Page Type
Cleared 510(K)
510(k) Number
K151437
510(k) Type
Traditional
Applicant
Atrium Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2015
Days to Decision
90 days
Submission Type
Summary

ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug

Page Type
Cleared 510(K)
510(k) Number
K151437
510(k) Type
Traditional
Applicant
Atrium Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2015
Days to Decision
90 days
Submission Type
Summary