# K953484: Pollux OA/Pollux 30A/Pollux 70A

- Pathway: 510(k) (Traditional)
- Applicant: Pollux Endoscopy, Inc.
- Decided: Sep 1, 1995 after 38 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.
21 later devices descend from it; 1 cites it directly.
0 of 22 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
- K082841: Spinal Foraminoscope (2009), 20 descendants of its own
- K130778: Discoscopes, Cervical Endoscopes (2014), 14 descendants of its own
- K180766: Endiscope, Endiscope Cervical (2018), 12 descendants of its own
- K201134: Arthrex NanoScope System (2020), 11 descendants of its own
- K243008: Arthrex NanoScope System (2025), 4 descendants of its own

Source page: https://510kreport.com/device/K953484
Methodology: https://510kreport.com/methodology