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FDA 510(k)

Biomet Microfixation OmniMax MMF System

K-Number: K202969 · 2021-08-05

ApplicantBiomet Microfixation
Decision Date2021-08-05
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Biomet Microfixation OmniMax MMF System is a medical device manufactured by Biomet Microfixation. It received FDA 510(k) clearance on 2021-08-05 under approval number K202969. 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 OmniMax MMF System?

Biomet Microfixation OmniMax MMF System is a medical device that received FDA 510(k) clearance on 2021-08-05. It is manufactured by Biomet Microfixation. The 510(k) number is K202969.

When was Biomet Microfixation OmniMax MMF System approved by the FDA?

Biomet Microfixation OmniMax MMF System received FDA 510(k) clearance on 2021-08-05, under approval number K202969.

What company makes Biomet Microfixation OmniMax MMF System?

Biomet Microfixation OmniMax MMF System is manufactured by Biomet Microfixation.

What is the FDA product code for Biomet Microfixation OmniMax MMF System?

The FDA product code for Biomet Microfixation OmniMax MMF System is JEY.

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Other Devices by Biomet Microfixation

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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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