# K951354: Olympus Arthroscopy System

- Pathway: 510(k) (Traditional)
- Applicant: Olympus America, Inc.
- Decided: Jun 14, 1995 after 82 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K982133: Olympus Endoscopic System Lumbar Hernia Discectomy and Its Ancillary Equipment (1998), 1 descendant of its own
- K160249: ULTRA Telescopes (2016), 0 descendants of its own
- K043128: Olympus Endoarm (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K951354
Methodology: https://510kreport.com/methodology