FDA 510(k)

Neuspera 神经刺激系统（NNS）

K号: K202781 · 2021-08-27

决定日期2021-08-27

产品代码GZF

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决定实质等同

器械摘要

Neuspera Neurostimulation System (NNS) is the device name listed in this FDA 510(k) record. The listed applicant is Neuspera Medical, Inc.. It received FDA 510(k) clearance on 2021-08-27 under 510(k) number K202781. The device is classified under product code GZF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Neuspera Neurostimulation System (NNS)?

Neuspera Neurostimulation System (NNS) is a medical device that received FDA 510(k) clearance on 2021-08-27. The listed applicant is Neuspera Medical, Inc.. The 510(k) number is K202781.

When did Neuspera Neurostimulation System (NNS) receive FDA 510(k) clearance?

Neuspera Neurostimulation System (NNS) received FDA 510(k) clearance on 2021-08-27, under 510(k) number K202781.

Who is the listed applicant for Neuspera Neurostimulation System (NNS)?

The FDA 510(k) record lists Neuspera Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Neuspera Neurostimulation System (NNS)?

The FDA product code for Neuspera Neurostimulation System (NNS) is GZF.

列明Neuspera Medical, 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。

K221303Neuspera Nuity 系统

官方来源

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