# K191259: Stryker CrossFlow Integrated Arthroscopy Pump

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Jul 12, 2019 after 63 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: 6 generations back to K950035 (1996). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123441: Stryker Crossflow Arthroscopy Pump, Stryker Endoscopy (2013) Summary page 4.

## Indications for use
The Stryker CrossFlow Integrated Arthroscopy Pump is a dual arthroscopic pump systein intended to provide fluid distension and irrigation of the knee, shoulder, hip, elbow, ankle and wrist joint cavities and fluid suction during diagnostic and operative arthroscopic procedures.

Source page: https://510kreport.com/device/K191259
Methodology: https://510kreport.com/methodology