# K922285: Agc and Maxim Knee Components with NTS

- Pathway: 510(k) (Traditional)
- Applicant: Biomet, Inc.
- Decided: Aug 13, 1992 after 90 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.
6 later devices descend from it; 3 cite it directly.
0 of 7 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
- K984331: Odi Ultimate Compression Hip Screw (1999), 3 descendants of its own
- K033286: Odi Talon Long Proximal Femoral Nail System (2004), 2 descendants of its own
- K111352: Talon Distalfix Proximal Femoral Nail (2011), 1 descendant of its own
- K223933: Exactech Equinoxe PHx Fracture System; Exactech EPIC Screws (2023), 0 descendants of its own
- K102367: Optigen Total Knee System (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K922285
Methodology: https://510kreport.com/methodology