FDA 510(k)

Neodent Implant System - Temporary Abutments

K-번호: K191191 · 2019-12-05

신청자Jjgc Industria E Comercio DE Materiais Dentarios S.A.

결정일2019-12-05

제품 코드NHA

자문 위원회DE

결정Substantially Equivalent

기기 요약

Neodent Implant System - Temporary Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2019-12-05 under 510(k) number K191191. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Neodent Implant System - Temporary Abutments?

Neodent Implant System - Temporary Abutments is a medical device that received FDA 510(k) clearance on 2019-12-05. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K191191.

When did Neodent Implant System - Temporary Abutments receive FDA 510(k) clearance?

Neodent Implant System - Temporary Abutments received FDA 510(k) clearance on 2019-12-05, under 510(k) number K191191.

Who is the listed applicant for Neodent Implant System - Temporary Abutments?

The FDA 510(k) record lists Jjgc Industria E Comercio DE Materiais Dentarios S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Neodent Implant System - Temporary Abutments?

The FDA product code for Neodent Implant System - Temporary Abutments is NHA.

Jjgc Industria E Comercio DE Materiais Dentarios S.A.를 신청인으로 등재한 기타 기록

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