# K173039: TruMatch CMF Titanium 3D Printed Implant

- Pathway: 510(k) (Traditional)
- Applicant: Materialise NV
- Decided: Jul 10, 2018 after 285 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: 2 generations back to K063790 (2007). 4 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170272: TruMatch CMF Titanium 3D Printed Implant System, Materialise NV (2017) Summary page 5.

## Most influential descendants
- K233874: tmCMF Solution (2024), 0 descendants of its own
- K232889: METICULY Patient-specific titanium maxillofacial mesh implant (2024), 0 descendants of its own

## Indications for use
The TruMatch CMF Titanium 3D Printed Implant is a patient specific implant and is intended for bone fixation and reconstruction, restoration of bone defects and intended to provide continuity in regions where the bone is missing and/or to augment the bone by means of an onlay device in the maxillofacial skeleton, midface and chin.

Source page: https://510kreport.com/device/K173039
Methodology: https://510kreport.com/methodology