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TRABECULAR METAL ACETABULAR REVISION SYSTEM CEMENTED CONTRAINED LINER

K072121 Class II Traditional
Decision Date
2008-01-07
Sponsor / Applicant
Zimmer, Inc.

Technical Specification

510(k) Submission ID K072121
Product Code KWZ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3310
Decision Date 2008-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRABECULAR METAL ACETABULAR REVISION SYSTEM CEMENTED CONTRAINED LINER received FDA 510(k) clearance under submission number K072121, sponsored by Zimmer, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code KWZ and 21 CFR 888.3310, within the Orthopedic review panel as a Class II device.