OsteoReady 牙齿种植系统
K号: K173575 · 2018-08-17
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决定日期2018-08-17
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
OsteoReady Dental Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Osteoready, LLC. It received FDA 510(k) clearance on 2018-08-17 under 510(k) number K173575. 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 OsteoReady Dental Implant System?
OsteoReady Dental Implant System is a medical device that received FDA 510(k) clearance on 2018-08-17. The listed applicant is Osteoready, LLC. The 510(k) number is K173575.
When did OsteoReady Dental Implant System receive FDA 510(k) clearance?
OsteoReady Dental Implant System received FDA 510(k) clearance on 2018-08-17, under 510(k) number K173575.
Who is the listed applicant for OsteoReady Dental Implant System?
The FDA 510(k) record lists Osteoready, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OsteoReady Dental Implant System?
The FDA product code for OsteoReady Dental Implant System is DZE.
相关临床试验
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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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