# K230533: Motive™ Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Cymedica Orthopedics, Inc.
- Decided: Mar 22, 2023 after 23 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K945676 (1995). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140586: Ascend Electrode, Neurometrix, Inc. (2014) Summary page 4.

## Indications for use
The Motive™ Electrode is intended for use as a disposable, conductive, and adhesive interface between the user’s skin and an electrical muscle stimulator. Motive Electrode is intended for adults of 22 years of age and older.

Source page: https://510kreport.com/device/K230533
Methodology: https://510kreport.com/methodology