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SMALL HIGH SPEED MOTOR DRILL SYSTEM

K030172 Class II Traditional
Decision Date
2003-04-03
Sponsor / Applicant
Brasseler USA I, L.P.

Technical Specification

510(k) Submission ID K030172
Product Code HBE
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4310
Decision Date 2003-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMALL HIGH SPEED MOTOR DRILL SYSTEM received FDA 510(k) clearance under submission number K030172, sponsored by Brasseler USA I, L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2003-04-03.

Classification & Regulation

This clearance is catalogued under FDA product code HBE and 21 CFR 882.4310, within the Neurology review panel as a Class II device.