刺激器，电的，植入的，用于尿失禁
PMA编号：P970004 · 2026-09-14
广告
决定日期2026-09-14
PMA 编号P970004
产品代码EZW
设备分类第3类
医疗专科G
法规编号21 CFR 8
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
器械摘要
Stimulator, electrical, implantable, for incontinence is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Neuromodulation. It received FDA 510(k) clearance on 2026-09-14. The device is classified under product code EZW. It was reviewed by the GU advisory panel.
常见问题
What is the Stimulator, electrical, implantable, for incontinence?
Stimulator, electrical, implantable, for incontinence is a medical device that received FDA 510(k) clearance on 2026-09-14. The listed applicant is Medtronic Neuromodulation.
When did Stimulator, electrical, implantable, for incontinence receive FDA 510(k) clearance?
The clearance date for Stimulator, electrical, implantable, for incontinence can be found in the official FDA records.
刺激器，电植入式，用于尿失禁，的列名申请人是谁？
The FDA 510(k) record lists Medtronic Neuromodulation as the applicant. This does not by itself establish the device manufacturer.
什么是用于尿失禁的植入式电刺激器的FDA产品代码？
FDA产品代码为Stimulator，electrical，implantable，用于尿失禁的刺激器是EZW。
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。
广告