# K962075: HSW GMBH Arthroscope

- Pathway: 510(k) (Traditional)
- Applicant: Henke Sass Wolf of America, Inc.
- Decided: Jan 17, 1997 after 234 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.
22 later devices descend from it; 1 cites it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K080560: Henke Sass Wolf of America Arthroscope (2008), 21 descendants of its own
- K093677: Stryker Arthroscope (2010), 11 descendants of its own
- K181819: SMARTRELEASE Endoscopic Soft Tissue Release System (2018), 6 descendants of its own
- K100577: Acclarent Cyclops Multi-Angle Endoscope (2011), 4 descendants of its own
- K110097: Acclarent Cyclops Multi-Angle Endoscope (2011), 3 descendants of its own

Source page: https://510kreport.com/device/K962075
Methodology: https://510kreport.com/methodology