POROUS COATED DISCOVERY ELBOW
K-Number: K051975 · 2005-09-06
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Device Summary
Frequently Asked Questions
What is the POROUS COATED DISCOVERY ELBOW?
POROUS COATED DISCOVERY ELBOW is a medical device that received FDA 510(k) clearance on 2005-09-06. The listed applicant is Biomet, Inc.. The 510(k) number is K051975.
When did POROUS COATED DISCOVERY ELBOW receive FDA 510(k) clearance?
POROUS COATED DISCOVERY ELBOW received FDA 510(k) clearance on 2005-09-06, under 510(k) number K051975.
Who is the listed applicant for POROUS COATED DISCOVERY ELBOW?
The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POROUS COATED DISCOVERY ELBOW?
The FDA product code for POROUS COATED DISCOVERY 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 Biomet, 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.
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