# K093677: Stryker Arthroscope

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Mar 5, 2010 after 98 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: 4 generations back to K833587 (1983). 15 ancestors in all.
11 later devices descend from it; 5 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080560: Henke Sass Wolf of America Arthroscope, Henke Sass Wolf of America, Inc. (2008) Summary page 3.

## Most influential descendants
- K100577: Acclarent Cyclops Multi-Angle Endoscope (2011), 4 descendants of its own
- K110097: Acclarent Cyclops Multi-Angle Endoscope (2011), 3 descendants of its own
- K140903: Nuvis Arthroscope (2014), 2 descendants of its own
- K202659: Stryker Arthroscope (2020), 1 descendant of its own
- K132433: Acclarent Cyclops Multi-Angle Endoscope (2014), 1 descendant 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 (carpel tunnel syndrome), temporal mandibular joint, ankle, elbow, and feet (plantar fascia release). No known contraindications.

Source page: https://510kreport.com/device/K093677
Methodology: https://510kreport.com/methodology