Nanovis 椎间融合系统及 FortiCore®
K号: K160874 · 2016-06-28
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器械摘要
常见问题
What is the Nanovis Intervertebral Body Fusion System and FortiCore®?
Nanovis Intervertebral Body Fusion System and FortiCore® is a medical device that received FDA 510(k) clearance on 2016-06-28. The listed applicant is Nanovis, LLC. The 510(k) number is K160874.
When did Nanovis Intervertebral Body Fusion System and FortiCore® receive FDA 510(k) clearance?
Nanovis Intervertebral Body Fusion System and FortiCore® received FDA 510(k) clearance on 2016-06-28, under 510(k) number K160874.
Who is the listed applicant for Nanovis Intervertebral Body Fusion System and FortiCore®?
The FDA 510(k) record lists Nanovis, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nanovis Intervertebral Body Fusion System and FortiCore®?
The FDA product code for Nanovis Intervertebral Body Fusion System and FortiCore® is MAX.
相关临床试验
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。
列明Nanovis, LLC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:MAX)
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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