# K173501: Meridian Vaginal Positioning System (VPS)

- Pathway: 510(k) (Traditional)
- Applicant: Coloplast
- Decided: Feb 9, 2018 after 88 days
- Product code: PWK (Instrumentation, Surgical Mesh, Urogynecologic, Transabdominal Repair Of Pelvic Organ Prolapse)
- Device class: 2
- Regulation: 21 CFR 884.4910
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K931386 (1993). 39 ancestors in all.
No later device cites it as a predicate yet.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140116: Restorelle Y Contour Mesh, Coloplast A/S (2014) Summary page 4.

## Indications for use
The Meridian VPS is a single-use device intended to assist in the position and manipulation of the vagina during gynecologic surgical procedures such as sacrocolpopexy.

Source page: https://510kreport.com/device/K173501
Methodology: https://510kreport.com/methodology