# K901940: Luhr Micro Mesh

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Corp.
- Decided: Sep 6, 1990 after 129 days
- Product code: JEY (Plate, Bone)
- Device class: 2
- Regulation: 21 CFR 872.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K973484: Chin Distractor (1997), 1 descendant of its own
- K030790: Osteomed Alveolar Distraction System (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K901940
Methodology: https://510kreport.com/methodology