Neodent Implant System Custom Abutments
K-Number: K233857 · 2024-05-02
Decision Date2024-05-02
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Neodent Implant System Custom Abutments is a medical device manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A.. It received FDA 510(k) clearance on 2024-05-02 under approval number K233857. 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 Neodent Implant System Custom Abutments?
Neodent Implant System Custom Abutments is a medical device that received FDA 510(k) clearance on 2024-05-02. It is manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K233857.
When was Neodent Implant System Custom Abutments approved by the FDA?
Neodent Implant System Custom Abutments received FDA 510(k) clearance on 2024-05-02, under approval number K233857.
What company makes Neodent Implant System Custom Abutments?
Neodent Implant System Custom Abutments is manufactured by JJGC Indústria e Comércio de Materiais Dentários S.A..
What is the FDA product code for Neodent Implant System Custom Abutments?
The FDA product code for Neodent Implant System Custom 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.