BIOMET'S MINIMALLY CONSTRAINED ELBOW
K-Number: K003253 · 2001-01-12
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Device Summary
Frequently Asked Questions
What is the BIOMET'S MINIMALLY CONSTRAINED ELBOW?
BIOMET'S MINIMALLY CONSTRAINED ELBOW is a medical device that received FDA 510(k) clearance on 2001-01-12. The listed applicant is Biomet, Inc.. The 510(k) number is K003253.
When did BIOMET'S MINIMALLY CONSTRAINED ELBOW receive FDA 510(k) clearance?
BIOMET'S MINIMALLY CONSTRAINED ELBOW received FDA 510(k) clearance on 2001-01-12, under 510(k) number K003253.
Who is the listed applicant for BIOMET'S MINIMALLY CONSTRAINED 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 BIOMET'S MINIMALLY CONSTRAINED ELBOW?
The FDA product code for BIOMET'S MINIMALLY CONSTRAINED 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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