meddevicedb.com FDA Device Reference

MTA2.1 MATERIAL

K140955 Class II Special
Decision Date
2014-06-11
Sponsor / Applicant
Avalon Biomed, Inc.

Technical Specification

510(k) Submission ID K140955
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2014-06-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTA2.1 MATERIAL received FDA 510(k) clearance under submission number K140955, sponsored by Avalon Biomed, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.