FDA 510(k)

Nexstim 导航脑刺激 (NBS) 6 系统 (NBS6)

K号: K252358 · 2026-03-20

决定日期2026-03-20

产品代码OBP

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决定实质等同

器械摘要

Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6) is the device name listed in this FDA 510(k) record. The listed applicant is Nexstim Oyj. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K252358. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6)?

Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6) is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Nexstim Oyj. The 510(k) number is K252358.

When did Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6) receive FDA 510(k) clearance?

Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6) received FDA 510(k) clearance on 2026-03-20, under 510(k) number K252358.

Who is the listed applicant for Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6)?

The FDA 510(k) record lists Nexstim Oyj as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6)?

The FDA product code for Nexstim Navigated Brain Stimulation (NBS) 6 System (NBS6) is OBP.

列明Nexstim Oyj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。

K253098Nexstim 导航脑刺激 (NBS) 6 系统 (NBS6)

官方来源

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