# K884837: Kinemax Tibial Wedge

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Corp.
- Decided: Feb 17, 1989 after 91 days
- Product code: HRY (Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3530
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K964951: Kinemax Plus Tibial Spacers (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K884837
Methodology: https://510kreport.com/methodology