# K932677: Axiom Total Knee System

- Pathway: 510(k) (Traditional)
- Applicant: Orthomet, Inc.
- Decided: Oct 14, 1994 after 499 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.
9 later devices descend from it; 2 cite it directly.
0 of 10 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
- K142550: EVOLUTION MP Revision Femur, EVOLUTION Femoral Augments (2014), 8 descendants of its own
- K182125: EVOLUTION Stemmed CS Femur (2018), 3 descendants of its own
- K171389: EVOLUTION Revision CCK System (2017), 3 descendants of its own
- K243574: Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique (2025), 1 descendant of its own
- K253728: EVOLUTION® AM BIOFOAM® Tibial System (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K932677
Methodology: https://510kreport.com/methodology