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MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM

K013772 Class II Special
Decision Date
2001-12-03
Sponsor / Applicant
Howmedica Osteonics

Technical Specification

510(k) Submission ID K013772
Product Code LXT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2001-12-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM received FDA 510(k) clearance under submission number K013772, sponsored by Howmedica Osteonics. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-12-03.

Classification & Regulation

This clearance is catalogued under FDA product code LXT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.