# K990443: Arthro-Surgimat-2000 Ecu

- Pathway: 510(k) (Special)
- Applicant: W.O.M. World of Medicine GmbH
- Decided: Feb 26, 1999 after 15 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: 3 generations back to K950035 (1996). 7 ancestors in all.
30 later devices descend from it; 2 cite it directly.
0 of 38 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983910: Arthro-Surgimat-1500, W.O.M. World of Medicine GmbH (1998) Summary page 1.
- K981859: Surgiflator-20 Ecu, W.O.M. World of Medicine GmbH (1998) Summary page 1.
- K933873: Concept Universal Pump System, Linvatec Corp. (1994) Summary page 1.

## Most influential descendants
- K030402: Arthroscopy Pump, Model A107 (2003), 29 descendants of its own
- K062380: Flosimple Arthroscopy Pump A120 (2006), 15 descendants of its own
- K112642: Aquilex Fluid Control System H112 (2012), 14 descendants of its own
- K123732: Hysteroscopy Pump HM6 (2013), 6 descendants of its own
- K123441: Stryker Crossflow Arthroscopy Pump (2013), 5 descendants of its own

## Indications for use
The Arthro-Surgimat-2000 ECU is a high flow arthroscopic pump intended for fluid distention of the knee, shoulder, elbow, ankle and wrist joint cavities under optional voice-activation control during arthroscopic procedures. (21 C.F.R. & 888.1100).

Source page: https://510kreport.com/device/K990443
Methodology: https://510kreport.com/methodology