COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN
K-Number: K973357 · 1998-03-02
Advertisement
Device Summary
Frequently Asked Questions
What is the COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN?
COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN is a medical device that received FDA 510(k) clearance on 1998-03-02. The listed applicant is Zimmer, Inc.. The 510(k) number is K973357.
When did COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN receive FDA 510(k) clearance?
COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN received FDA 510(k) clearance on 1998-03-02, under 510(k) number K973357.
Who is the listed applicant for COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN?
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 TOTAL ELBOW, NEW HINGE PIN?
The FDA product code for COONRAD/MORREY TOTAL ELBOW, NEW HINGE PIN 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement