# K062380: Flosimple Arthroscopy Pump A120

- Pathway: 510(k) (Special)
- Applicant: W.O.M. World of Medicine AG
- Decided: Dec 14, 2006 after 121 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K950035 (1996). 13 ancestors in all.
15 later devices descend from it; 1 cites it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030402: Arthroscopy Pump, Model A107, W.O.M. World of Medicine AG (2003) Summary page 1.
- K000153: Arthro-Surgimat-A103, W.O.M. World of Medicine GmbH (2000) Summary page 1.
- K983910: Arthro-Surgimat-1500, W.O.M. World of Medicine GmbH (1998) Summary page 1.
- K990732: Lap-Wave 3000 (P07), W.O.M. World of Medicine GmbH (1999) Summary page 1.

## Most influential descendants
- K112642: Aquilex Fluid Control System H112 (2012), 14 descendants of its own
- K123732: Hysteroscopy Pump HM6 (2013), 6 descendants of its own
- K190372: Aveta System (2019), 4 descendants of its own
- K180735: Endomat Select (2018), 2 descendants of its own
- K180825: Fluent Fluid Management System (2018), 2 descendants of its own

## Recalls of this device
- May 24, 2024 · Class II · Z-2243-2024: Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery

## Indications for use
The FLOSIMPLE Arthroscopy Pump A120 is intended to provide fluid distension and irrigation of the knee, shoulder, hip, elbow, ankle and wrist joint cavities during diagnostic and operative arthroscopic procedures.

Source page: https://510kreport.com/device/K062380
Methodology: https://510kreport.com/methodology