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ConvertX Nephroureteral Stent System

Page Type
Cleared 510(K)
510(k) Number
K161277
510(k) Type
Traditional
Applicant
BRIGHTWATER MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
200 days
Submission Type
Summary

ConvertX Nephroureteral Stent System

Page Type
Cleared 510(K)
510(k) Number
K161277
510(k) Type
Traditional
Applicant
BRIGHTWATER MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
200 days
Submission Type
Summary