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BREAST VOLUME NAVIGATOR

Page Type
Cleared 510(K)
510(k) Number
K141870
510(k) Type
Traditional
Applicant
METRITRACK LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2014
Days to Decision
27 days
Submission Type
Summary

BREAST VOLUME NAVIGATOR

Page Type
Cleared 510(K)
510(k) Number
K141870
510(k) Type
Traditional
Applicant
METRITRACK LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2014
Days to Decision
27 days
Submission Type
Summary