Last synced on 14 November 2025 at 11:06 pm

Vortek Single Loop Ureteral Stent

Page Type
Cleared 510(K)
510(k) Number
K201436
510(k) Type
Traditional
Applicant
Coloplast Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2021
Days to Decision
269 days
Submission Type
Summary

Vortek Single Loop Ureteral Stent

Page Type
Cleared 510(K)
510(k) Number
K201436
510(k) Type
Traditional
Applicant
Coloplast Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2021
Days to Decision
269 days
Submission Type
Summary