meddevicedb.com FDA Device Reference

COSMATRIX

K060829 Class II Abbreviated
Decision Date
2006-05-17
Sponsor / Applicant
Tei Biosciences, Inc.

Technical Specification

510(k) Submission ID K060829
Product Code FTM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2006-05-17
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COSMATRIX received FDA 510(k) clearance under submission number K060829, sponsored by Tei Biosciences, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2006-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code FTM and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.