# K130169: FMS Vue Fluid Managment System, FMS Connect Interface Cable

- Pathway: 510(k) (Traditional)
- Applicant: Depuy Mitek, A Johnson & Johnson Company
- Decided: May 1, 2013 after 97 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K954465 (1995). 2 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954465: FMS Duo, Future Medical Systems, Inc. (1995) Summary page 1.
- K002040: FMS Solo, Future Medical Systems, Inc. (2000) Summary page 1.

## Most influential descendants
- K192921: Zeos Aqua Vision Pump and tube (2020), 2 descendants of its own
- K203480: DOUBLEFLO system (2021), 1 descendant of its own
- K233675: FMS VUE™ Fluid Management and Tissue Debridement System (2024), 0 descendants of its own
- K221919: DOUBLEFLO INFLOW/OUTFLOW PUMP, accessories and tubing sets (2023), 0 descendants of its own
- K171237: FMS VUE II Fluid Management and Tissue Debridement System (2018), 0 descendants of its own

## Indications for use
DePuy Mitek FMS VUE Fluid Management and Tissue Debridement System is intended to provide controlled fluid distention and suction, controlled cutting, burring, shaving and abrading of bone and tissue for use in arthroscopic surgery of the shoulder, knee, ankle, elbow, wrist and hip joints. The FMS CONNECT Interface Cables are accessories to the DePuy Mitek FMS Fluid Management and Tissue Debridement Systems; they connect competitive shavers to FMS arthroscopy pumps.

Source page: https://510kreport.com/device/K130169
Methodology: https://510kreport.com/methodology