# K955884: Coordinate Revision Knee System

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Mar 13, 1996 after 76 days
- Product code: JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) DePuy AMK Landmark Revision Knee System and Full Wedge Tibial Tray (renamed the Coordinate Revision Knee System): named in the summary without a submission number
- (no number) Johnson & Johnson P.F.C. Modular Knee System: named in the summary without a submission number
- (no number) DePuy Synatomic Variable Fit Tibial Plateau: named in the summary without a submission number
- (no number) DePuy AMK Congruency PS Tibial Inserts: named in the summary without a submission number

## Most influential descendants
- K982585: Depuy Amk Total Knee System Depuy Coordinate Ultra Knee Revision System (1998), 0 descendants of its own

## Indications for use
The DePuy Coordinate II Revision Knee System is indicated for use with bone cement as either a primary or revision tricompartmental knee replacement system.

Source page: https://510kreport.com/device/K955884
Methodology: https://510kreport.com/methodology