# K211847: AdVance XP Male Sling System

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corporation
- Decided: Dec 20, 2021 after 188 days
- Product code: OTM (Mesh, Surgical, For Stress Urinary Incontinence, Male)
- Device class: 2
- Regulation: 21 CFR 878.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K931386 (1993). 33 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182169: AdVance XP Male Sling, Boston Scientific Corporation (2018) Summary page 4.

## Most influential descendants
- K242960: AdVance™ XP Male Sling System (720163-03) (2024), 0 descendants of its own

## Indications for use
The AdVance™ XP Male Sling System is intended for the treatment of male stress urinary incontinence (SUI) by the placement of a suburethral sling.

Source page: https://510kreport.com/device/K211847
Methodology: https://510kreport.com/methodology