# K030648: Vectorsurge 5 Model 470

- Pathway: 510(k) (Special)
- Applicant: Metron Medical Australia, Pty, Ltd.
- Decided: Mar 28, 2003 after 28 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- 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
Relief of chronic intractable pain, acute post traumatic pain or acute post surgical pain (TNS Mode); Relaxation of muscle spasm (Interferential Mode); Prevention or retardation of disuse atrophy (Interferential Mode); Increasing local blood flow (Interferential Mode); Muscle re-education (Interferential Mode); Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis (Interferential Mode); and Maintaining or increasing range of motion (Interferential Mode).

Source page: https://510kreport.com/device/K030648
Methodology: https://510kreport.com/methodology