# K024291: Arthrex Continuous Wave Iii Arthoscopy Pump, Model AR-6475

- Pathway: 510(k) (Traditional)
- Applicant: Arthrex, Inc.
- Decided: Mar 20, 2003 after 86 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.
5 later devices descend from it; 2 cite 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)
- None. The FDA summary names its predicate without a number.
- (no number) AR-6400 Arthrex arthroscopic pump: named in the summary without a submission number
- (no number) AR-6300 Arthrex arthroscopic pump: named in the summary without a submission number

## Most influential descendants
- K083707: Arthrex Dual Wave Arthroscopy Fluid Management Device (2009), 3 descendants of its own
- 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
- K151932: Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing (2016), 0 descendants of its own

## Indications for use
The Arthrex Continuous Wave Ill Arthroscopy Pump 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/K024291
Methodology: https://510kreport.com/methodology