# K983910: Arthro-Surgimat-1500

- Pathway: 510(k) (Special)
- Applicant: W.O.M. World of Medicine GmbH
- Decided: Nov 25, 1998 after 22 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: 2 generations back to K912453 (1991). 3 ancestors in all.
31 later devices descend from it; 3 cite 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)
- K962114: Arthro-Surgimat, W.O.M. World of Medicine GmbH (1996) Summary page 1.

## Most influential descendants
- K990443: Arthro-Surgimat-2000 Ecu (1999), 30 descendants of its own
- 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

## Indications for use
The Arthro-Surgimat-1500 is a high flow arthroscopic pump intended for fluid distention of the knee, shoulder, elbow, ankle, and wrist joint cavities during arthroscopic procedures.

Source page: https://510kreport.com/device/K983910
Methodology: https://510kreport.com/methodology