FDA 510(k)

THE Graft Collagen

K号: K230305 · 2024-07-24

决定日期2024-07-24

产品代码NPM

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决定实质等同

器械摘要

THE Graft Collagen is the device name listed in this FDA 510(k) record. The listed applicant is Purgo Biologics, Inc.. It received FDA 510(k) clearance on 2024-07-24 under 510(k) number K230305. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the THE Graft Collagen?

THE Graft Collagen is a medical device that received FDA 510(k) clearance on 2024-07-24. The listed applicant is Purgo Biologics, Inc.. The 510(k) number is K230305.

When did THE Graft Collagen receive FDA 510(k) clearance?

THE Graft Collagen received FDA 510(k) clearance on 2024-07-24, under 510(k) number K230305.

Who is the listed applicant for THE Graft Collagen?

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

What is the FDA product code for THE Graft Collagen?

The FDA product code for THE Graft Collagen is NPM.

列明Purgo Biologics, 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。

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