GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study

Inclusion Criteria

• •Subjects who satisfy all of the following criteria will be considered eligible for enrollment in this study:
• •1. Female subjects who had laparotomic or laparoscopic abdominal sacrocolpopexy, including robotic-assisted, for apical vaginal or uterine prolapse
• •2. GYNEMESH PS Mesh was used as a bridging material according to the IFU.
• •3. Able and willing to participate in follow-up
• •4. Subject or authorized representative has signed the approved informed consent