# K182090: AposTherapy System

- Pathway: 510(k) (Traditional)
- Applicant: Apos Medical Assets, Ltd.
- Decided: Nov 16, 2018 after 106 days
- Product code: QDT (Shoe With Adjustable Sole Units)
- Device class: 1
- Regulation: 21 CFR 890.3475
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The AposTherapy System is intended to be used by trained professionals for adjusting the distribution of weight/force(s) that is being applied to a lower limb. The AposTherapy System is intended for patients with knee osteoarthritis, to help temporarily reduce knee pain and improve lower extremity function during activities of daily living.

Source page: https://510kreport.com/device/K182090
Methodology: https://510kreport.com/methodology