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KNIFE BLADE TIP

K823911 Class I Traditional
Decision Date
1983-01-21
Sponsor / Applicant
Treace Medical, Inc.

Technical Specification

510(k) Submission ID K823911
Product Code JYO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4420
Decision Date 1983-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KNIFE BLADE TIP received FDA 510(k) clearance under submission number K823911, 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 1983-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code JYO and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.