INTELLIO SHIFT 系统
K号: K232290 · 2023-12-11
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器械摘要
常见问题
What is the INTELLIO SHIFT System?
INTELLIO SHIFT System is a medical device that received FDA 510(k) clearance on 2023-12-11. The listed applicant is ArthroCare Corporation. The 510(k) number is K232290.
When did INTELLIO SHIFT System receive FDA 510(k) clearance?
INTELLIO SHIFT System received FDA 510(k) clearance on 2023-12-11, under 510(k) number K232290.
Who is the listed applicant for INTELLIO SHIFT System?
The FDA 510(k) record lists ArthroCare Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTELLIO SHIFT System?
The FDA product code for INTELLIO SHIFT System is GEI.
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ArthroCare Corporation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:GEI)
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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