SD 牙槽钉
K号: K173570 · 2019-05-17
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决定日期2019-05-17
产品代码NHA
咨询委员会DE
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器械摘要
SD Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Surgident Co., Ltd.. It received FDA 510(k) clearance on 2019-05-17 under 510(k) number K173570. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SD Abutment?
SD Abutment is a medical device that received FDA 510(k) clearance on 2019-05-17. The listed applicant is Surgident Co., Ltd.. The 510(k) number is K173570.
When did SD Abutment receive FDA 510(k) clearance?
SD Abutment received FDA 510(k) clearance on 2019-05-17, under 510(k) number K173570.
Who is the listed applicant for SD Abutment?
The FDA 510(k) record lists Surgident Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SD Abutment?
The FDA product code for SD Abutment is NHA.
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。
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。
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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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