CAMLOG 和 CONELOG Abutments for Screw-retained Restorations (ASR)
K号: K152509 · 2016-01-12
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器械摘要
常见问题
What is the CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?
CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is a medical device that received FDA 510(k) clearance on 2016-01-12. The listed applicant is Altatec GmbH. The 510(k) number is K152509.
When did CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) receive FDA 510(k) clearance?
CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) received FDA 510(k) clearance on 2016-01-12, under 510(k) number K152509.
Who is the listed applicant for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?
The FDA 510(k) record lists Altatec GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)?
The FDA product code for CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR) is NHA.
相关临床试验
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列明Altatec GmbH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。
相关器械(代码:NHA)
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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