# K150742: Muscle Stimulation System 110

- Pathway: 510(k) (Special)
- Applicant: Niveus Medical, Inc.
- Decided: Jul 23, 2015 after 122 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: 5 generations back to K010782 (2001). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123642: Muscle Stimulation System, Niveus Medical, Inc. (2013) Summary page 4.

## Indications for use
The Niveus Medical Muscle Stimulation System 110 is indicated for: 1) Maintaining or increasing range of motion of the knee joint 2) Prevention or retardation of disuse atrophy in the quadriceps 3) Muscle re-education of the quadriceps 4) Relaxation of muscle spasms 5) Increasing local blood circulation

Source page: https://510kreport.com/device/K150742
Methodology: https://510kreport.com/methodology