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FDA 510(k)

BIOMET MICROFIXATION FACIAL PLATING SYSTEM

K-Number: K121589 · 2012-09-21

Decision Date2012-09-21
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIOMET MICROFIXATION FACIAL PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Microfixation. It received FDA 510(k) clearance on 2012-09-21 under 510(k) number K121589. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOMET MICROFIXATION FACIAL PLATING SYSTEM?

BIOMET MICROFIXATION FACIAL PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2012-09-21. The listed applicant is Biomet Microfixation. The 510(k) number is K121589.

When did BIOMET MICROFIXATION FACIAL PLATING SYSTEM receive FDA 510(k) clearance?

BIOMET MICROFIXATION FACIAL PLATING SYSTEM received FDA 510(k) clearance on 2012-09-21, under 510(k) number K121589.

Who is the listed applicant for BIOMET MICROFIXATION FACIAL PLATING SYSTEM?

The FDA 510(k) record lists Biomet Microfixation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOMET MICROFIXATION FACIAL PLATING SYSTEM?

The FDA product code for BIOMET MICROFIXATION FACIAL PLATING SYSTEM is JEY.

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 Microfixation 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: JEY)

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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