# K223027: NeuroTrigger Basic (NTB)

- Pathway: 510(k) (Traditional)
- Applicant: Neurotrigger
- Decided: Oct 10, 2023 after 376 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K912178 (1991). 19 ancestors in all.
No later device cites it as a predicate yet.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193275: Nerve and Muscle Stimulator, Shenzhen Xft Medical Limited (2020) Summary page 6.

## Indications for use
NeuroTrigger Basic is indicated for the prevention or retardation of disuse atrophy, muscle re-education, and for maintaining or increasing range of motion.

Source page: https://510kreport.com/device/K223027
Methodology: https://510kreport.com/methodology