meddevicedb.com FDA Device Reference

SIS PLASTIC SURGERY MATRIX

K034039 Class II Traditional
Decision Date
2004-02-18
Sponsor / Applicant
Cook Biotech, Inc.

Technical Specification

510(k) Submission ID K034039
Product Code FTM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2004-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIS PLASTIC SURGERY MATRIX received FDA 510(k) clearance under submission number K034039, sponsored by Cook Biotech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2004-02-18.

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.