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BETACONE HIP PROSTHESIS SYSTEM

K051826 Class II Traditional
Decision Date
2005-11-18
Sponsor / Applicant
Waldemar Link GmbH & Co. KG

Technical Specification

510(k) Submission ID K051826
Product Code LWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 2005-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BETACONE HIP PROSTHESIS SYSTEM received FDA 510(k) clearance under submission number K051826, sponsored by Waldemar Link GmbH & Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code LWJ and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.