mXACT 全髋关节假体偏心组件,mXACT 全髋关节假体中心组件和 mXACT PRO 全髋关节假体套装
K号: K241269 · 2025-01-17
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器械摘要
常见问题
What is the mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit?
mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit is a medical device that received FDA 510(k) clearance on 2025-01-17. The listed applicant is MED-EL Elektromedizinische Geräte GmbH. The 510(k) number is K241269.
When did mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit receive FDA 510(k) clearance?
mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit received FDA 510(k) clearance on 2025-01-17, under 510(k) number K241269.
Who is the listed applicant for mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit?
The FDA 510(k) record lists MED-EL Elektromedizinische Geräte GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit?
The FDA product code for mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit is ETA.
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。
列明MED-EL Elektromedizinische Geräte 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:ETA)
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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