# K083707: Arthrex Dual Wave Arthroscopy Fluid Management Device

- Pathway: 510(k) (Traditional)
- Applicant: Arthrex, Inc.
- Decided: Aug 3, 2009 after 231 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 K954465 (1995). 2 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024291: Arthrex Continuous Wave Iii Arthoscopy Pump, Model AR-6475, Arthrex, Inc. (2003) Summary page 1.
- K954465: FMS Duo, Future Medical Systems, Inc. (1995) Summary page 1.

## Most influential descendants
- K180735: Endomat Select (2018), 2 descendants of its own
- K201355: Endomat Select, IBS Shaver Software, License (2020), 1 descendant of its own
- K261706: Endomat Select (UP220) (2026), 0 descendants of its own

## Indications for use
The Arthrex Dual Wave Arthroscopy Fluid Management Device is intended to provide consistent, non-pulsing control of intra-articular irrigation and distention pressuring during all phases of arthroscopic surgery.

Source page: https://510kreport.com/device/K083707
Methodology: https://510kreport.com/methodology