# K170773: Stryker Universal Mesh

- Pathway: 510(k) (Traditional)
- Applicant: Stryker
- Decided: Nov 8, 2017 after 239 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: 4 generations back to K954385 (1996). 11 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022185: Universal CMF System, Stryker Instruments (2002) Summary page 5.

## Most influential descendants
- K182425: Universal Mesh - Sterile (2018), 0 descendants of its own

## Indications for use
The Universal Mesh is indicated for non-load-bearing reconstruction in the maxillofacial skeleton of patients in whom skeletal growth is complete.

Source page: https://510kreport.com/device/K170773
Methodology: https://510kreport.com/methodology