FDA 510(k)

Zfx Abutments

Numéro K : K231915 · 2024-03-01

Date de décision2024-03-01

Code produitNHA

Comité consultatifDE

DécisionSubstantially Equivalent

Résumé du dispositif

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

Questions fréquentes

What is the Zfx Abutments?

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

When did Zfx Abutments receive FDA 510(k) clearance?

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

Who is the listed applicant for Zfx Abutments?

The FDA 510(k) record lists Zfx GmbH - A Company of Zimvie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zfx Abutments?

The FDA product code for Zfx Abutments is NHA.

Essais cliniques associés

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Dispositifs connexes (Code : NHA)

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Source officielle

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