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DISTAL VOLAR RADIUS PLATING SYSTEMS

K112345 Class II Traditional
Decision Date
2011-10-31
Sponsor / Applicant
Medos International SARL

Technical Specification

510(k) Submission ID K112345
Product Code LXT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2011-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISTAL VOLAR RADIUS PLATING SYSTEMS received FDA 510(k) clearance under submission number K112345, sponsored by Medos International SARL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-10-31.

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.