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TREACE DRILL SYSTEM

K862807 Class II Traditional
Decision Date
1986-08-15
Sponsor / Applicant
Treace Medical, Inc.

Technical Specification

510(k) Submission ID K862807
Product Code ERL
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4250
Decision Date 1986-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TREACE DRILL SYSTEM received FDA 510(k) clearance under submission number K862807, sponsored by Treace Medical, 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 1986-08-15.

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.