# K932070: Duracon Stabilizer Femoral Component and Insert

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Corp.
- Decided: Mar 22, 1995 after 693 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.
11 later devices descend from it; 5 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K994207: Howmedica Osteonics Modular Rotating Hinge Knee (2000), 6 descendants of its own
- K223069: Modular Rotating Hinge Knee Systems and Compatible Components (2023), 4 descendants of its own
- K223528: Triathlon® Hinge Knee System (2023), 4 descendants of its own
- K230416: Triathlon® Hinge Knee System; Triathlon® Revision Insert X3® (2023), 3 descendants of its own
- K251665: Triathlon® Hinge Knee System (2025), 2 descendants of its own

Source page: https://510kreport.com/device/K932070
Methodology: https://510kreport.com/methodology