# K070336: Stockert Neuro N50, MODEL12267

- Pathway: 510(k) (Traditional)
- Applicant: Stockert GmbH
- Decided: Jun 14, 2007 after 129 days
- Product code: GXD (Generator, Lesion, Radiofrequency)
- Device class: 2
- Regulation: 21 CFR 882.4400
- 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 K896450 (1991). 1 ancestor in all.
5 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K896450: Neuro N 50 Lesion Generator, Leibinger & Fischer, Ltd. (1991) Summary page 1.

## Most influential descendants
- K171143: Relievant Medsystems RF Generator (2017), 4 descendants of its own
- K190504: Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator (2019), 3 descendants of its own
- K213836: Intracept Intraosseous Nerve Ablation System (2022), 1 descendant of its own
- K250213: OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Dual Kit) (2025), 0 descendants of its own
- K222281: Intracept Intraosseous Nerve Ablation System (2022), 0 descendants of its own

## Indications for use
Stockert NEURO N5b is a RF generator for general high frequency applications: 1. Lesioning nerve tissue for functional neurosurgical procedures; or 2. Radiofrequency heat lesion procedures for the relief of pain; or 3. Stimulation procedures like provoking stimulation, localized stimulation, blocking stimulation or intraoperative test stimulation

Source page: https://510kreport.com/device/K070336
Methodology: https://510kreport.com/methodology