FDA 510(k)

ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM

K-Number: K021891 · 2002-09-05

Decision Date2002-09-05

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2002-09-05 under 510(k) number K021891. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM?

ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-05. The listed applicant is Zimmer, Inc.. The 510(k) number is K021891.

When did ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM receive FDA 510(k) clearance?

ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM received FDA 510(k) clearance on 2002-09-05, under 510(k) number K021891.

Who is the listed applicant for ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM?

The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM?

The FDA product code for ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM is LPH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.