# K950045: KLS-Martin Mandibular Fracture/Reconstruction System

- Pathway: 510(k) (Traditional)
- Applicant: Karl Leibinger GmbH U. Co. KG
- Decided: Mar 23, 1995 after 77 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.
438 later devices descend from it; 2 cite it directly.
0 of 439 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
- K032442: KLS-Martin Mandibular/Reconstruction System II (2003), 435 descendants of its own
- K040598: KLS Martin Hand Plating System (2004), 360 descendants of its own
- K050868: Maxlock (2005), 343 descendants of its own
- K073624: Modular Foot System (2008), 342 descendants of its own
- K100618: Maxlock Extreme Extremity Plating System with Variable Angle Technology (2010), 339 descendants of its own

Source page: https://510kreport.com/device/K950045
Methodology: https://510kreport.com/methodology