meddevicedb.com FDA Device Reference

SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM

K113567 Class II Traditional
Decision Date
2012-11-19
Sponsor / Applicant
Synthes, Inc.

Technical Specification

510(k) Submission ID K113567
Product Code JEY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4760
Decision Date 2012-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNTHES MATRIXMADIBLE PLATE AND SCREW SYSTEM received FDA 510(k) clearance under submission number K113567, sponsored by Synthes, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code JEY and 21 CFR 872.4760, within the Dental review panel as a Class II device.