SPiN 胸部导航系统
K号: K170023 · 2017-05-15
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器械摘要
SPiN Thoracic Navigation System is the device name listed in this FDA 510(k) record. The listed applicant is Veran Medical Technologies, Inc.. It received FDA 510(k) clearance on 2017-05-15 under 510(k) number K170023. 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 SPiN Thoracic Navigation System?
SPiN Thoracic Navigation System is a medical device that received FDA 510(k) clearance on 2017-05-15. The listed applicant is Veran Medical Technologies, Inc.. The 510(k) number is K170023.
When did SPiN Thoracic Navigation System receive FDA 510(k) clearance?
SPiN Thoracic Navigation System received FDA 510(k) clearance on 2017-05-15, under 510(k) number K170023.
Who is the listed applicant for SPiN Thoracic Navigation System?
The FDA 510(k) record lists Veran Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPiN Thoracic Navigation System?
The FDA product code for SPiN Thoracic Navigation System is JAK.
相关临床试验
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列明Veran Medical Technologies, Inc.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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