c1Trac
K号: K222912 · 2023-05-16
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决定日期2023-05-16
产品代码ITH
咨询委员会PM
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决定实质等同
器械摘要
c1Trac is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2023-05-16 under 510(k) number K222912. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the c1Trac?
c1Trac is a medical device that received FDA 510(k) clearance on 2023-05-16. The listed applicant is Zimmer Medizinsysteme GmbH. The 510(k) number is K222912.
When did c1Trac receive FDA 510(k) clearance?
c1Trac received FDA 510(k) clearance on 2023-05-16, under 510(k) number K222912.
Who is the listed applicant for c1Trac?
The FDA 510(k) record lists Zimmer Medizinsysteme GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for c1Trac?
The FDA product code for c1Trac is ITH.
列明Zimmer Medizinsysteme 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：ITH）
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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