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FDA 510(k)

Zfx Abutments

K-Number: K231915 · 2024-03-01

ApplicantZfx GmbH - A Company of Zimvie
Decision Date2024-03-01
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Zfx Abutments is a medical device manufactured by Zfx GmbH - A Company of Zimvie. It received FDA 510(k) clearance on 2024-03-01 under approval number K231915. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Zfx Abutments?

Zfx Abutments is a medical device that received FDA 510(k) clearance on 2024-03-01. It is manufactured by Zfx GmbH - A Company of Zimvie. The 510(k) number is K231915.

When was Zfx Abutments approved by the FDA?

Zfx Abutments received FDA 510(k) clearance on 2024-03-01, under approval number K231915.

What company makes Zfx Abutments?

Zfx Abutments is manufactured by Zfx GmbH - A Company of Zimvie.

What is the FDA product code for Zfx Abutments?

The FDA product code for Zfx Abutments is NHA.

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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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