FDA 510(k)

Neodent Implant System – Custom Abutments

Numéro K : K233857 · 2024-05-02

DemandeurJJGC Indústria e Comércio de Materiais Dentários S.A.

Date de décision2024-05-02

Code produitNHA

Comité consultatifDE

DécisionSubstantially Equivalent

Résumé du dispositif

Neodent Implant System – Custom Abutments is the device name listed in this FDA 510(k) record. The listed applicant is JJGC Indústria e Comércio de Materiais Dentários S.A.. It received FDA 510(k) clearance on 2024-05-02 under 510(k) number K233857. 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 Neodent Implant System – Custom Abutments?

Neodent Implant System – Custom Abutments is a medical device that received FDA 510(k) clearance on 2024-05-02. The listed applicant is JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K233857.

When did Neodent Implant System – Custom Abutments receive FDA 510(k) clearance?

Neodent Implant System – Custom Abutments received FDA 510(k) clearance on 2024-05-02, under 510(k) number K233857.

Who is the listed applicant for Neodent Implant System – Custom Abutments?

The FDA 510(k) record lists JJGC Indústria e Comércio de Materiais Dentários S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Neodent Implant System – Custom Abutments?

The FDA product code for Neodent Implant System – Custom Abutments is NHA.

Essais cliniques associés

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Dispositifs connexes (Code : NHA)

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Source officielle

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