meddevicedb.com FDA Device Reference

Argulated Locking Plates

K143338 Class II Special
Decision Date
2015-04-01
Sponsor / Applicant
Osteomed LP

Technical Specification

510(k) Submission ID K143338
Product Code JEY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4760
Decision Date 2015-04-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Argulated Locking Plates received FDA 510(k) clearance under submission number K143338, sponsored by Osteomed LP. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-04-01.

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.