# K070272: Neuroport Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Cyberkinetics Neurotechnology Systems, Inc.
- Decided: Aug 3, 2007 after 186 days
- Product code: GZL (Electrode, Depth)
- Device class: 2
- Regulation: 21 CFR 882.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K042384 (2005). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042384: Neuroport Recording Microelectrode Array System, Cyberkinetics, Inc. (Cki) (2005) Summary page 1.

## Most influential descendants
- K110010: Neuroport Cortical Microelectrode Array System (2011), 0 descendants of its own

## Indications for use
The intended use of the Cyberkinetics Neurotechnology Systems, Inc. NeuroPort Microelectrode Array System is for temporary (< 30 days) recording and monitoring of brain electrical activity.

Source page: https://510kreport.com/device/K070272
Methodology: https://510kreport.com/methodology