# K243020: MIDASVu

- Pathway: 510(k) (Traditional)
- Applicant: Intravu, Inc.
- Decided: Dec 2, 2024 after 66 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: 10 generations back to K833587 (1983). 43 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181982: MIDAScope and Introducer Kit, and MIDASystem, Intravu, Inc. (2018) Summary page 5.

## Most influential descendants
- K252579: Orthoscan TAU MVP Mini C-Arm System (2026), 0 descendants of its own

## Indications for use
The MIDASVu is indicated for use in diagnostic and operative arthroscopic and endoscopic procedures to provide illumination and visualization of interior cavity joints and other body cavities through a natural or surgical opening.

Source page: https://510kreport.com/device/K243020
Methodology: https://510kreport.com/methodology