# K011387: Neurotherm, Model JK4

- Pathway: 510(k) (Traditional)
- Applicant: Eurolink, LLC
- Decided: Sep 6, 2001 after 122 days
- Product code: GXI (Probe, Radiofrequency Lesion)
- Device class: 2
- Regulation: 21 CFR 882.4725
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K090608: Minta Ryan RF Thermocouple Electrode (Ryan-50, 100, 150 and 200), Minta Intermediate Cable (Ryan-C, -R, -B) (2010), 0 descendants of its own

## Recalls of this device
- Jul 28, 2008 · Not classified · Z-0838-2009: Distal tip may detach from the probe

Source page: https://510kreport.com/device/K011387
Methodology: https://510kreport.com/methodology