FDA 510(k)

HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE

K-Number: K902436 · 1990-08-29

Decision Date1990-08-29

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent for Some Indications

Device Summary

HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K902436. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE?

HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Zimmer, Inc.. The 510(k) number is K902436.

When did HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE receive FDA 510(k) clearance?

HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE received FDA 510(k) clearance on 1990-08-29, under 510(k) number K902436.

Who is the listed applicant for HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE?

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/TINIDIUM SURFACE?

The FDA product code for HG MULTILOCK HIP PROSTHESIS W/TINIDIUM SURFACE is JDI.

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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.