# K151932: Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corporation
- Decided: Mar 31, 2016 after 261 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 K024291 (2003). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 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 4.

## Indications for use
The Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing are used in conjunction with the CrossFlow Integrated Arthroscopy Pump (K123441) to provide fluid distension and irrigation of the knee, shoulder, hip, elbow, ankle, and wrist joint cavities during diagnostic and operative arthroscopic procedures.

Source page: https://510kreport.com/device/K151932
Methodology: https://510kreport.com/methodology