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ROSENBERG SKIN GRAFTING KNIVES

K842702 Class I Traditional
Decision Date
1984-08-02
Sponsor / Applicant
Downs Surgical , Ltd.

Technical Specification

510(k) Submission ID K842702
Product Code GFD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1984-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROSENBERG SKIN GRAFTING KNIVES received FDA 510(k) clearance under submission number K842702, sponsored by Downs Surgical , Ltd.. 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 1984-08-02.

Classification & Regulation

This clearance is catalogued under FDA product code GFD and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.