# K032052: UC-Plus Solution Unicondylar Knee

- Pathway: 510(k) (Special)
- Applicant: Plus Orthopedics
- Decided: Jul 25, 2003 after 23 days
- Product code: HRY (Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3530
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K954481 (1996). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982859: UC-Plus Solution Unicondylar Knee System, Plus Orthopedics (1999) Summary page 1.

## Recalls of this device
- Jul 18, 2006 · Not classified · Z-0192-2007: The modified devices were distributed by Plus Orthopedics USA (Plus USA) June 10, 2003 prior to FDA approval to market of the modified device (Special 510(k) K032052, clearance date July 25, 2003) and

## Indications for use
The UC-PLUS Solution Unicondylar Knee is intended for use in uni-compartmental degenerative arthritis, local osteonecrosis of the femoral condyle, light to medium uni-compartmental destruction of the knee joint due to idiopathic and post-traumatic degenerative arthritis, traumatic uni-compartmental bone and/or cartilage lesions. It is intended for use with bone cement only.

Source page: https://510kreport.com/device/K032052
Methodology: https://510kreport.com/methodology