meddevicedb.com FDA Device Reference

PNEUMATIC POWERED BUR

K780139 Class I Traditional
Decision Date
1978-02-01
Sponsor / Applicant
North Palm Beach Orthodepic Assoc.

Technical Specification

510(k) Submission ID K780139
Product Code HSZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1978-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PNEUMATIC POWERED BUR received FDA 510(k) clearance under submission number K780139, sponsored by North Palm Beach Orthodepic Assoc.. 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 1978-02-01.

Classification & Regulation

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