The purpose of this study is to monitor the use of Virtue® Male Sling in a real world population and collect medical data on effectiveness and to monitor safety of Virtue® at 12 and 36 months post device implantation in men with post-prostatectomy urinary incontinence.
Implanted with the Virtue® Male Sling System
Refuses to be included in the survey or that their medical data will be used for research purposes.
Indication for the Virtue® Male Sling System implantation is not for the treatment of male urinary incontinence