Straumann RN Gold Abutment for Bridge
K号: K151590 · 2016-03-04
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决定日期2016-03-04
产品代码NHA
咨询委员会DE
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决定实质等同
器械摘要
Straumann RN Gold Abutment for Bridge is the device name listed in this FDA 510(k) record. The listed applicant is Straumann USA, LLC. It received FDA 510(k) clearance on 2016-03-04 under 510(k) number K151590. 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 Straumann RN Gold Abutment for Bridge?
Straumann RN Gold Abutment for Bridge is a medical device that received FDA 510(k) clearance on 2016-03-04. The listed applicant is Straumann USA, LLC. The 510(k) number is K151590.
When did Straumann RN Gold Abutment for Bridge receive FDA 510(k) clearance?
Straumann RN Gold Abutment for Bridge received FDA 510(k) clearance on 2016-03-04, under 510(k) number K151590.
Who is the listed applicant for Straumann RN Gold Abutment for Bridge?
The FDA 510(k) record lists Straumann USA, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Straumann RN Gold Abutment for Bridge?
The FDA product code for Straumann RN Gold Abutment for Bridge is NHA.
相关临床试验
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列明Straumann USA, 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：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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