颅内动脉瘤血流导向装置
PMA编号：P170024 · 2026-08-28
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决定日期2026-08-28
PMA 编号P170024
产品代码OUT
设备分类第3类
医疗专科U
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
器械摘要
Intracranial aneurysm flow diverter is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovascular. It received FDA 510(k) clearance on 2026-08-28. The device is classified under product code OUT. It was reviewed by the NE advisory panel.
常见问题
What is the Intracranial aneurysm flow diverter?
Intracranial aneurysm flow diverter is a medical device that received FDA 510(k) clearance on 2026-08-28. The listed applicant is Stryker Neurovascular.
When did Intracranial aneurysm flow diverter receive FDA 510(k) clearance?
The clearance date for Intracranial aneurysm flow diverter can be found in the official FDA records.
颅内动脉瘤血流导向装置的申请人名单是谁？
The FDA 510(k) record lists Stryker Neurovascular as the applicant. This does not by itself establish the device manufacturer.
颅内动脉瘤血流导向装置的FDA产品代码是什么？
FDA产品代码为颅内动脉瘤血流导向装置的是OUT。
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。
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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