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FDA 510(k)

COONRAD III TOTAL ELBOW

K-Number: K883665 · 1989-02-03

ApplicantZimmer, Inc.
Decision Date1989-02-03
Product CodeJDC
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

COONRAD III TOTAL ELBOW is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K883665. The device is classified under product code JDC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the COONRAD III TOTAL ELBOW?

COONRAD III TOTAL ELBOW is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Zimmer, Inc.. The 510(k) number is K883665.

When did COONRAD III TOTAL ELBOW receive FDA 510(k) clearance?

COONRAD III TOTAL ELBOW received FDA 510(k) clearance on 1989-02-03, under 510(k) number K883665.

Who is the listed applicant for COONRAD III TOTAL ELBOW?

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 III TOTAL ELBOW?

The FDA product code for COONRAD III TOTAL ELBOW 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.

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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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