Last synced on 25 November 2022 at 11:04 pm

Vortek Single Loop Ureteral Stent

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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