# K050473: RBK Patella Femoral Knee

- Pathway: 510(k) (Traditional)
- Applicant: Global Orthopaedic Technology, USA, Inc.
- Decided: Nov 14, 2005 after 263 days
- Product code: KRR (Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3540
- 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 RBK Patella Femoral Knee is intended for use in treating patients with osteoarthritis in the distal femur and patella, patients with a history of patellar dislocation or patellar fracture and those patients with failed previous surgery where pain, deformity or dysfunction persists. The device is a single-use implant that is intended for use with bone cement.

Source page: https://510kreport.com/device/K050473
Methodology: https://510kreport.com/methodology