# K112064: Resorb X-G

- Pathway: 510(k) (Traditional)
- Applicant: KLS-Martin L.P.
- Decided: Mar 23, 2012 after 248 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
Longest line of descent: 8 generations back to K904436 (1990). 31 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080862: Sonicweld RX (Resorb-X), KLS-Martin L.P. (2008) Summary page 1.
- K062789: Synthes (Usa) Rapid Resorbable Fixation System, Synthes (Usa) (2007) Summary page 2.
- K992355: Lactosorb Trauma Plating System, Biomet, Inc. (1999) Summary page 1.

## Most influential descendants
- K133304: RXG Distraction System (2014), 0 descendants of its own
- K121606: Resorb-X G (2013), 0 descendants of its own

## Indications for use
The KLS Martin Resorb-X G is intended for use in non-load bearing fracture repair and reconstructive procedures in adolescent and adult populations. In addition, resorbable meshes, plates and pins may be used in non-load bearing applications for maintaining the relative position of, and/or containing, bony fragments, bone grafts (autograft or allograft), or bone graft substitutes in oral and maxillofacial reconstruction.

Source page: https://510kreport.com/device/K112064
Methodology: https://510kreport.com/methodology