# K202659: Stryker Arthroscope

- Pathway: 510(k) (Special)
- Applicant: Stryker
- Decided: Dec 1, 2020 after 78 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: 5 generations back to K833587 (1983). 17 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093677: Stryker Arthroscope, Stryker Endoscopy (2010) Summary page 4.
- K183470: Precision Ideal Eyes Arthroscopes, Stryker (2019) Summary page 4.

## Most influential descendants
- K254103: HOPKINS Telescopes for Arthroscopy (2026), 0 descendants of its own

## Indications for use
Stryker Arthroscopes are endoscopic devices introduced into a patient to provide an internal view or image of the interior of a joint for examination, diagnosis, and/or therapy. Arthroscopes are indicated for use in arthroscopic procedures performed in the hip, knee, shoulder, wrist (carpal tunnel syndrome), temporal mandibular joint, ankle elbow, and feet (plantar fascia release).

Source page: https://510kreport.com/device/K202659
Methodology: https://510kreport.com/methodology