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FDA 510(k)

COONRAD/MORREY ELBOW CEMENT RESTRICTOR

K-Number: K040389 · 2004-05-17

ApplicantZimmer, Inc.
Decision Date2004-05-17
Product CodeJDC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COONRAD/MORREY ELBOW CEMENT RESTRICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2004-05-17 under 510(k) number K040389. The device is classified under product code JDC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COONRAD/MORREY ELBOW CEMENT RESTRICTOR?

COONRAD/MORREY ELBOW CEMENT RESTRICTOR is a medical device that received FDA 510(k) clearance on 2004-05-17. The listed applicant is Zimmer, Inc.. The 510(k) number is K040389.

When did COONRAD/MORREY ELBOW CEMENT RESTRICTOR receive FDA 510(k) clearance?

COONRAD/MORREY ELBOW CEMENT RESTRICTOR received FDA 510(k) clearance on 2004-05-17, under 510(k) number K040389.

Who is the listed applicant for COONRAD/MORREY ELBOW CEMENT RESTRICTOR?

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 COONRAD/MORREY ELBOW CEMENT RESTRICTOR?

The FDA product code for COONRAD/MORREY ELBOW CEMENT RESTRICTOR is JDC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Zimmer, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 344 devices →

Related Devices (Code: JDC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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