FDA 510(k)

HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM

K-Number: K921308 · 1994-02-22

Decision Date1994-02-22

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K921308. 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 HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM?

HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Zimmer, Inc.. The 510(k) number is K921308.

When did HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM receive FDA 510(k) clearance?

HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM received FDA 510(k) clearance on 1994-02-22, under 510(k) number K921308.

Who is the listed applicant for HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM?

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 HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM?

The FDA product code for HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM 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.