meddevicedb.com FDA Device Reference

SURGICAL BUR

K872475 Class I Traditional
Decision Date
1987-07-02
Sponsor / Applicant
Tava Surgical Instruments

Technical Specification

510(k) Submission ID K872475
Product Code GFF
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1987-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL BUR received FDA 510(k) clearance under submission number K872475, sponsored by Tava Surgical Instruments. 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 1987-07-02.

Classification & Regulation

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