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ConvertX Biliary Stent System

Page Type
Cleared 510(K)
510(k) Number
K181669
510(k) Type
Traditional
Applicant
BrightWater Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2019
Days to Decision
262 days
Submission Type
Summary

ConvertX Biliary Stent System

Page Type
Cleared 510(K)
510(k) Number
K181669
510(k) Type
Traditional
Applicant
BrightWater Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2019
Days to Decision
262 days
Submission Type
Summary