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MyoSure MANUAL Tissue Removal Device

Page Type
Cleared 510(K)
510(k) Number
K173901
510(k) Type
Traditional
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2018
Days to Decision
137 days
Submission Type
Summary

MyoSure MANUAL Tissue Removal Device

Page Type
Cleared 510(K)
510(k) Number
K173901
510(k) Type
Traditional
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2018
Days to Decision
137 days
Submission Type
Summary