FDA 510(k)

LW植入系统 - 支撑装置

K号: K233167 · 2024-03-25

决定日期2024-03-25

产品代码NHA

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决定实质等同

器械摘要

LW Implant System – Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Ossvis Co., Ltd.. It received FDA 510(k) clearance on 2024-03-25 under 510(k) number K233167. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LW Implant System – Abutment?

LW Implant System – Abutment is a medical device that received FDA 510(k) clearance on 2024-03-25. The listed applicant is Ossvis Co., Ltd.. The 510(k) number is K233167.

When did LW Implant System – Abutment receive FDA 510(k) clearance?

LW Implant System – Abutment received FDA 510(k) clearance on 2024-03-25, under 510(k) number K233167.

Who is the listed applicant for LW Implant System – Abutment?

The FDA 510(k) record lists Ossvis Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LW Implant System – Abutment?

The FDA product code for LW Implant System – Abutment is NHA.

列明Ossvis Co., Ltd.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。

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相关器械（代码：NHA）

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。

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官方来源

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