# K220738: Motive Knee Wrap

- Pathway: 510(k) (Traditional)
- Applicant: Cymedica Orthopedics, Inc.
- Decided: May 12, 2022 after 59 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: 8 generations back to K010335 (2001). 39 ancestors in all.
No later device cites it as a predicate yet.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210604: Intellihab System, Cymedica Orthopedics, Inc. (2021) Summary page 11.
- K192733: RelieforMe TENS/EMS Device Model UPK-GE01, Umeheal, Ltd. (2019) Summary page 11.

## Indications for use
The Motive™ Knee Wrap device is intended to strengthen the quadriceps muscle using powered muscle stimulation to provide symptomatic temporary pain relief associated with knee arthritis. The Motive™ Knee Wrap device is indicated for adults of 22 years of age and older.

Source page: https://510kreport.com/device/K220738
Methodology: https://510kreport.com/methodology