# K093717: C-Mor Visualization Device

- Pathway: 510(k) (Traditional)
- Applicant: Axis Surgical Technologies, Inc.
- Decided: Mar 2, 2010 after 90 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). 23 ancestors in all.
16 later devices descend from it; 2 cite it directly.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082293: Surgview Integrated Visualization System, Biovision Technologies, LLC (2008) Summary page 1.
- K043395: Smith & Nephew Videoarthroscope, Smith & Nephew, Inc. (2005) Summary page 1.
- K072879: Innervue Diagnostic Scope System, Biomet Orthopedics, Inc. (2008) Summary page 1.

## Most influential descendants
- K141119: Camera Enabled Probe (2014), 7 descendants of its own
- K102733: Vision-Sciences Ent-5000 Video Ent Scope with Endosheath Technology, Vision-Sciences Dpu-5000/Dpu-5050 Video Processor (2011), 7 descendants of its own
- K162475: mi-eye 2, mi-eye 2 monitor (2016), 6 descendants of its own
- K181982: MIDAScope and Introducer Kit, and MIDASystem (2018), 2 descendants of its own
- K243020: MIDASVu (2024), 1 descendant of its own

## Indications for use
The Axis Surgical Technologies C-MOR Visualization Device is indicated for use in diagnostic and operative arthroscopic and endoscopic procedures to provide illumination and visualization of an interior cavity of the body through either a natural or surgical opening.

Source page: https://510kreport.com/device/K093717
Methodology: https://510kreport.com/methodology