# K093062: Vertos Medical Mild Device Kit

- Pathway: 510(k) (Traditional)
- Applicant: X-Sten Corp.
- Decided: Feb 4, 2010 after 127 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 K922881 (1992). 39 ancestors in all.
13 later devices descend from it; 4 cite it directly.
0 of 53 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062038: X-Sten Mild Tool Kit, Model MTK-0001, X-Sten Corp. (2006) Summary page 1.
- K062711: Ultra Low Profile Rongeur, Baxano, Inc. (2007) Summary page 1.

## Most influential descendants
- K180876: DTRAX Spinal System (2018), 7 descendants of its own
- K190201: CORUS Spinal System (2019), 6 descendants of its own
- K212636: CORUS Spinal System-X (2021), 5 descendants of its own
- K240625: CORUS Navigation Access System (2024), 4 descendants of its own
- K233800: Vertos mild Device Kit (MDK-0002) (2024), 3 descendants of its own

## Indications for use
The Vertos Medical mild® Device Kit is a set of specialized surgical instruments intended to be used to perform lumbar decompressive procedures for the treatment of various spinal conditions.

Source page: https://510kreport.com/device/K093062
Methodology: https://510kreport.com/methodology