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UROLIFT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN130023
510(k) Type
Direct
Applicant
Neotract, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
9/13/2013
Days to Decision
190 days

UROLIFT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN130023
510(k) Type
Direct
Applicant
Neotract, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
9/13/2013
Days to Decision
190 days