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MODIFIED STERILIZATION OF DRILLS, BURRS, TREPHINES

K900388 Class II Traditional
Decision Date
1990-05-07
Sponsor / Applicant
Midas Rex Pneumatic Tools, Inc.

Technical Specification

510(k) Submission ID K900388
Product Code HBE
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4310
Decision Date 1990-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED STERILIZATION OF DRILLS, BURRS, TREPHINES received FDA 510(k) clearance under submission number K900388, sponsored by Midas Rex Pneumatic Tools, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1990-05-07.

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.