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FDA 510(k)

MODIFIED SINGLE AXLE TOTAL ELBOW

K-Number: K000683 · 2000-06-27

ApplicantBiomet, Inc.
Decision Date2000-06-27
Product CodeJDC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFIED SINGLE AXLE TOTAL 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 2000-06-27 under 510(k) number K000683. 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 MODIFIED SINGLE AXLE TOTAL ELBOW?

MODIFIED SINGLE AXLE TOTAL ELBOW is a medical device that received FDA 510(k) clearance on 2000-06-27. The listed applicant is Biomet, Inc.. The 510(k) number is K000683.

When did MODIFIED SINGLE AXLE TOTAL ELBOW receive FDA 510(k) clearance?

MODIFIED SINGLE AXLE TOTAL ELBOW received FDA 510(k) clearance on 2000-06-27, under 510(k) number K000683.

Who is the listed applicant for MODIFIED SINGLE AXLE TOTAL 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 MODIFIED SINGLE AXLE TOTAL ELBOW?

The FDA product code for MODIFIED SINGLE AXLE 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 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.

View all 418 devices →

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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