# K140903: Nuvis Arthroscope

- Pathway: 510(k) (Traditional)
- Applicant: Integrated Endoscopy, Inc.
- Decided: Jul 17, 2014 after 99 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: 5 generations back to K833587 (1983). 17 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093677: Stryker Arthroscope, Stryker Endoscopy (2010) Summary page 1.
- K933576: Arthroscope, Disposable, United States Surgical, A Division of Tyco Healthc (1994) Summary page 1.

## Most influential descendants
- K191594: Nuvis Battery Arthroscope (2019), 0 descendants of its own
- K152511: Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula (2016), 0 descendants of its own

## Indications for use
Integrated Endoscopy's NuVis™ 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™ 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/K140903
Methodology: https://510kreport.com/methodology