# K162459: AccuPoint Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Microprobes For Life Science, Inc. Dba Neuron
- Decided: Jun 15, 2017 after 286 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: 4 generations back to K811452 (1981). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033173: Micro Targeting Electrode, FHC, Inc. (2004) Summary page 4.
- K991522: Microtargeting Electrode, FHC, Inc. (2000) Summary page 4.

## Indications for use
Neuron AccuPoint™ Electrodes are intended for use in intraoperative recording of single unit neuronal activity or intraoperative stimulation of neural elements in the brain.

Source page: https://510kreport.com/device/K162459
Methodology: https://510kreport.com/methodology