# K962114: Arthro-Surgimat

- Pathway: 510(k) (Traditional)
- Applicant: W.O.M. World of Medicine GmbH
- Decided: Aug 22, 1996 after 83 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 K912453 (1991). 2 ancestors in all.
32 later devices descend from it; 1 cites 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)
- K933873: Concept Universal Pump System, Linvatec Corp. (1994) Summary page 1.
- K912453: Intelijet TM Fluid Management System, Smith & Nephew Dyonics, Inc. (1991) Summary page 1.

## Most influential descendants
- K983910: Arthro-Surgimat-1500 (1998), 31 descendants of its own
- 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

## Indications for use
The Arthro-Surgimat is a high flow arthroscopic pump classified under 21 C.F.R. § 888.1100 intended to distend joint cavities during arthroscopic procedures.

Source page: https://510kreport.com/device/K962114
Methodology: https://510kreport.com/methodology