FDA 510(k)

骨锚 (NGS-BA-01)

K号: K233703 · 2024-04-26

决定日期2024-04-26

产品代码HAW

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决定实质等同

器械摘要

Bone Anchor (NGS-BA-01) is the device name listed in this FDA 510(k) record. The listed applicant is ClearPoint Neuro, Inc.. It received FDA 510(k) clearance on 2024-04-26 under 510(k) number K233703. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Bone Anchor (NGS-BA-01)?

Bone Anchor (NGS-BA-01) is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is ClearPoint Neuro, Inc.. The 510(k) number is K233703.

When did Bone Anchor (NGS-BA-01) receive FDA 510(k) clearance?

Bone Anchor (NGS-BA-01) received FDA 510(k) clearance on 2024-04-26, under 510(k) number K233703.

Who is the listed applicant for Bone Anchor (NGS-BA-01)?

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

What is the FDA product code for Bone Anchor (NGS-BA-01)?

The FDA product code for Bone Anchor (NGS-BA-01) is HAW.

列明ClearPoint Neuro, 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。

K243657ClearPoint 系统（软件版本 3.0）K233144ClearPoint 骨螺钉标记物 K233141SmartFrame OR K233155ClearPointer 光学导航棒 K233243ClearPoint 系统（软件版本 2.2）K232102ClearPoint Array 系统（版本 1.2）

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官方来源

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