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FDA 510(k)

Biomet Microfixation RibFix Advantage System

K-Number: K203474 · 2021-01-28

ApplicantBiomet Micofixation
Decision Date2021-01-28
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Biomet Microfixation RibFix Advantage System is a medical device manufactured by Biomet Micofixation. It received FDA 510(k) clearance on 2021-01-28 under approval number K203474. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Biomet Microfixation RibFix Advantage System?

Biomet Microfixation RibFix Advantage System is a medical device that received FDA 510(k) clearance on 2021-01-28. It is manufactured by Biomet Micofixation. The 510(k) number is K203474.

When was Biomet Microfixation RibFix Advantage System approved by the FDA?

Biomet Microfixation RibFix Advantage System received FDA 510(k) clearance on 2021-01-28, under approval number K203474.

What company makes Biomet Microfixation RibFix Advantage System?

Biomet Microfixation RibFix Advantage System is manufactured by Biomet Micofixation.

What is the FDA product code for Biomet Microfixation RibFix Advantage System?

The FDA product code for Biomet Microfixation RibFix Advantage System is HRS.

Related Clinical Trials

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Related Devices (Code: HRS)

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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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