FDA 510(k)

Neodent Implant System - GM Zygomatic Implant System

K-번호: K232099 · 2023-10-31

신청자JJGC Indústria e Comércio de Materiais Dentários S.A.

결정일2023-10-31

제품 코드DZE

자문 위원회DE

결정Substantially Equivalent

기기 요약

Neodent Implant System - GM Zygomatic Implant System 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 2023-10-31 under 510(k) number K232099. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Neodent Implant System - GM Zygomatic Implant System?

Neodent Implant System - GM Zygomatic Implant System is a medical device that received FDA 510(k) clearance on 2023-10-31. The listed applicant is JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K232099.

When did Neodent Implant System - GM Zygomatic Implant System receive FDA 510(k) clearance?

Neodent Implant System - GM Zygomatic Implant System received FDA 510(k) clearance on 2023-10-31, under 510(k) number K232099.

Who is the listed applicant for Neodent Implant System - GM Zygomatic Implant System?

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 - GM Zygomatic Implant System?

The FDA product code for Neodent Implant System - GM Zygomatic Implant System is DZE.

JJGC Indústria e Comércio de Materiais Dentários S.A.를 신청인으로 등재한 기타 기록

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