Neodent Implant System
K号: K190958 · 2019-11-09
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决定日期2019-11-09
产品代码DZE
咨询委员会DE
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决定实质等同
器械摘要
Neodent Implant System 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 2019-11-09 under 510(k) number K190958. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Neodent Implant System?
Neodent Implant System is a medical device that received FDA 510(k) clearance on 2019-11-09. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K190958.
When did Neodent Implant System receive FDA 510(k) clearance?
Neodent Implant System received FDA 510(k) clearance on 2019-11-09, under 510(k) number K190958.
Who is the listed applicant for Neodent Implant System?
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?
The FDA product code for Neodent Implant System is DZE.
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列明Jjgc Industria E Comercio DE Materiais Dentarios S.A.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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相关器械（代码：DZE）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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