FDA 510(k)

递送器中的胶原蛋白和无机骨矿物质

K号: K171008 · 2017-10-30

决定日期2017-10-30

产品代码NPM

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决定实质等同

器械摘要

Anorganic Bone Mineral with Collagen in Delivery Applicator is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2017-10-30 under 510(k) number K171008. 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 Anorganic Bone Mineral with Collagen in Delivery Applicator?

Anorganic Bone Mineral with Collagen in Delivery Applicator is a medical device that received FDA 510(k) clearance on 2017-10-30. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K171008.

When did Anorganic Bone Mineral with Collagen in Delivery Applicator receive FDA 510(k) clearance?

Anorganic Bone Mineral with Collagen in Delivery Applicator received FDA 510(k) clearance on 2017-10-30, under 510(k) number K171008.

Who is the listed applicant for Anorganic Bone Mineral with Collagen in Delivery Applicator?

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

What is the FDA product code for Anorganic Bone Mineral with Collagen in Delivery Applicator?

The FDA product code for Anorganic Bone Mineral with Collagen in Delivery Applicator is NPM.

列明Collagen Matrix, 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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