# K070874: Arthro Kinetics Vesalius MR Generator, Models 2004-2006; Accessories for MR Generator

- Pathway: 510(k) (Traditional)
- Applicant: Arthro Kinetics, Inc.
- Decided: Nov 2, 2007 after 218 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Intended for resection, ablation, and coagulation of soft tissue and hemostasis of blood vessels in surgical procedures such as but not limited to orthopedic, arthroscopic, and spinal procedures.

Source page: https://510kreport.com/device/K070874
Methodology: https://510kreport.com/methodology