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ONCOBIONIC SYSTEM

K080376 Class II Traditional
Decision Date
2008-04-02
Sponsor / Applicant
Oncobionic Incorporated

Technical Specification

510(k) Submission ID K080376
Product Code OAB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2008-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONCOBIONIC SYSTEM received FDA 510(k) clearance under submission number K080376, sponsored by Oncobionic Incorporated. 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 2008-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code OAB and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.