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X-T AIR DRILL

K905800 Class II Traditional
Decision Date
1991-04-22
Sponsor / Applicant
Xomed-Treace, Inc.

Technical Specification

510(k) Submission ID K905800
Product Code ERL
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4250
Decision Date 1991-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-T AIR DRILL received FDA 510(k) clearance under submission number K905800, sponsored by Xomed-Treace, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1991-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code ERL and 21 CFR 874.4250, within the Ear, Nose, Throat review panel as a Class II device.