Stereotaxic Guiding Surgical Devices, NaoTrac S
K号: K242575 · 2025-05-23
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决定日期2025-05-23
产品代码HAW
咨询委员会NE
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器械摘要
Stereotaxic Guiding Surgical Devices, NaoTrac S is the device name listed in this FDA 510(k) record. The listed applicant is Brain Navi Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K242575. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Stereotaxic Guiding Surgical Devices, NaoTrac S?
Stereotaxic Guiding Surgical Devices, NaoTrac S is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Brain Navi Biotechnology Co., Ltd.. The 510(k) number is K242575.
When did Stereotaxic Guiding Surgical Devices, NaoTrac S receive FDA 510(k) clearance?
Stereotaxic Guiding Surgical Devices, NaoTrac S received FDA 510(k) clearance on 2025-05-23, under 510(k) number K242575.
Who is the listed applicant for Stereotaxic Guiding Surgical Devices, NaoTrac S?
The FDA 510(k) record lists Brain Navi Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stereotaxic Guiding Surgical Devices, NaoTrac S?
The FDA product code for Stereotaxic Guiding Surgical Devices, NaoTrac S is HAW.
相关临床试验
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相关器械（代码：HAW）
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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