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FDA 510(k)

BIOMET'S MINIMALLY CONSTRAINED ELBOW

K-Number: K003253 · 2001-01-12

ApplicantBiomet, Inc.
Decision Date2001-01-12
Product CodeJDC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOMET'S MINIMALLY CONSTRAINED ELBOW is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2001-01-12 under 510(k) number K003253. 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 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.

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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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