FDA 510(k)

SPRINT 周围神经刺激 (PNS) 系统

K号: K223306 · 2023-01-25

决定日期2023-01-25

产品代码NHI

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决定实质等同

器械摘要

SPRINT Peripheral Nerve Stimulation (PNS) System is the device name listed in this FDA 510(k) record. The listed applicant is Spr Therapeutics, Inc.. It received FDA 510(k) clearance on 2023-01-25 under 510(k) number K223306. The device is classified under product code NHI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SPRINT Peripheral Nerve Stimulation (PNS) System?

SPRINT Peripheral Nerve Stimulation (PNS) System is a medical device that received FDA 510(k) clearance on 2023-01-25. The listed applicant is Spr Therapeutics, Inc.. The 510(k) number is K223306.

When did SPRINT Peripheral Nerve Stimulation (PNS) System receive FDA 510(k) clearance?

SPRINT Peripheral Nerve Stimulation (PNS) System received FDA 510(k) clearance on 2023-01-25, under 510(k) number K223306.

Who is the listed applicant for SPRINT Peripheral Nerve Stimulation (PNS) System?

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

What is the FDA product code for SPRINT Peripheral Nerve Stimulation (PNS) System?

The FDA product code for SPRINT Peripheral Nerve Stimulation (PNS) System is NHI.

列明Spr Therapeutics, 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。

K240974SPRINT PNS 系统 K211801SPRINT PNS 系统 K202660SPRINT PNS 系统 K181422SPRINT 周围神经刺激系统，Extensa，SPRINT 周围神经刺激系统，Endura，SPRINT 临床编程器套件

官方来源

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