# K013982: Kinematch Patello-Femoral Resurfacing Impalant

- Pathway: 510(k) (Traditional)
- Applicant: Kinamed, Inc.
- Decided: May 21, 2002 after 169 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The KineMatch™ Patello-Femoral Resurfacing Implant is intended to be used in patellofemoral arthroplasty in patients with degenerative arthritis of the distal femur and patella, patients with a history of patellar dislocation or patella fracture, or patients with failed previous surgery where pain, deformity, or dysfunction persists. The KineMatch' Patello-Femoral Resurfacing Implant is intended to be articulated against the Gem' all-polyethylene patella implant (K994214). The KineMatch™ Patello-Femoral Resurfacing Implant is intended for use with bone cement.

Source page: https://510kreport.com/device/K013982
Methodology: https://510kreport.com/methodology