# K923802: Timesh Titanium Mini-Softplate/Screw

- Pathway: 510(k) (Traditional)
- Applicant: Ti-Mesh, Inc.
- Decided: Oct 26, 1992 after 89 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.
11 later devices descend from it; 4 cite it directly.
0 of 12 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
- K021684: The Bioplate Rigid Fixation Bone Plating System for Craniomaxillofacial Surgery (2002), 7 descendants of its own
- K062819: Bioplate Rigid Bone Plating System for Craniomaxillofacial Surgery (2006), 3 descendants of its own
- K073006: Osteotrans -MX Bioabsorbable Bone Fixation System (2008), 2 descendants of its own
- K023810: Modification to Bioplate Rigid Fixation Bone Plating System for Craniomaxillofacial Surgery (2002), 1 descendant of its own
- K022033: Sterile Plate & Screw Kit Configurations for Use with the Bioplate Titanium Fixation System (2002), 1 descendant of its own

Source page: https://510kreport.com/device/K923802
Methodology: https://510kreport.com/methodology