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MALLET, SURGICAL

K882349 Class I Traditional
Decision Date
1988-06-23
Sponsor / Applicant
Treace Medical, Inc.

Technical Specification

510(k) Submission ID K882349
Product Code HXL
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1988-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MALLET, SURGICAL received FDA 510(k) clearance under submission number K882349, sponsored by Treace Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1988-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code HXL and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.