RFG-01
K号: K240178 · 2024-07-15
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决定日期2024-07-15
产品代码PBX
咨询委员会SU
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决定实质等同
器械摘要
RFG-01 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 2024-07-15 under 510(k) number K240178. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the RFG-01?
RFG-01 is a medical device that received FDA 510(k) clearance on 2024-07-15. The listed applicant is Zimmer Medizinsysteme GmbH. The 510(k) number is K240178.
When did RFG-01 receive FDA 510(k) clearance?
RFG-01 received FDA 510(k) clearance on 2024-07-15, under 510(k) number K240178.
Who is the listed applicant for RFG-01?
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 RFG-01?
The FDA product code for RFG-01 is PBX.
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：PBX）
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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