# K943348: KLS Chin Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Patton, Boggs & Blow
- Decided: Oct 4, 1994 after 84 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K241314: KLS Martin Oral-Max Implants MR Conditional (bundled) (2024), 1 descendant of its own
- K260137: KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient Solutions (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K943348
Methodology: https://510kreport.com/methodology