# K000153: Arthro-Surgimat-A103

- Pathway: 510(k) (Special)
- Applicant: W.O.M. World of Medicine GmbH
- Decided: Feb 8, 2000 after 21 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
No predicates in its family tree.
16 later devices descend from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- 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
- K190372: Aveta System (2019), 4 descendants of its own
- K180735: Endomat Select (2018), 2 descendants of its own

Source page: https://510kreport.com/device/K000153
Methodology: https://510kreport.com/methodology