XACT 机器人系统
K号: K201586 · 2020-07-09
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器械摘要
XACT Robotic System is the device name listed in this FDA 510(k) record. The listed applicant is Xact Robotics, Ltd.. It received FDA 510(k) clearance on 2020-07-09 under 510(k) number K201586. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the XACT Robotic System?
XACT Robotic System is a medical device that received FDA 510(k) clearance on 2020-07-09. The listed applicant is Xact Robotics, Ltd.. The 510(k) number is K201586.
When did XACT Robotic System receive FDA 510(k) clearance?
XACT Robotic System received FDA 510(k) clearance on 2020-07-09, under 510(k) number K201586.
Who is the listed applicant for XACT Robotic System?
The FDA 510(k) record lists Xact Robotics, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XACT Robotic System?
The FDA product code for XACT Robotic System is JAK.
相关临床试验
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列明Xact Robotics, Ltd.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：JAK）
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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