# K110010: Neuroport Cortical Microelectrode Array System

- Pathway: 510(k) (Special)
- Applicant: Blackrock Microsystems, Inc.
- Decided: Feb 9, 2011 after 37 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: 2 generations back to K042384 (2005). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070272: Neuroport Electrode, Cyberkinetics Neurotechnology Systems, Inc. (2007) Summary page 2.

## Indications for use
The intended use of the Blackrock Neurosystems LLC, Neuroport TM Microelectrode Array System is for temporary (<30 days) recording and monitoring of brain electrical activity.

Source page: https://510kreport.com/device/K110010
Methodology: https://510kreport.com/methodology