# K191594: Nuvis Battery Arthroscope

- Pathway: 510(k) (Special)
- Applicant: Integrated Endoscopy, Inc.
- Decided: Jul 11, 2019 after 24 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: 6 generations back to K833587 (1983). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140903: Nuvis Arthroscope, Integrated Endoscopy, Inc. (2014) Summary page 4.

## Indications for use
Integrated Endoscopy’s Nuvis® Battery Arthroscope is an endoscopic device introduced into a patient to provide an internal view or image of the interior of a joint for examination, diagnosis, and/or therapy. Integrated Endoscopy’s Nuvis® Battery Arthroscopes are indicated for use in arthroscopic procedures performed in the knee, shoulder, hip, wrist (carpel tunnel syndrome), temporal mandibular joint, ankle, elbow, and feet (plantar fascia release).

Source page: https://510kreport.com/device/K191594
Methodology: https://510kreport.com/methodology