FDA 510(k)

猪矿物质胶原蛋白复合物可塑型

K号: K201859 · 2020-09-11

决定日期2020-09-11

产品代码NPM

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决定实质等同

器械摘要

Porcine Mineral Collagen Composite Moldable 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 2020-09-11 under 510(k) number K201859. 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 Porcine Mineral Collagen Composite Moldable?

Porcine Mineral Collagen Composite Moldable is a medical device that received FDA 510(k) clearance on 2020-09-11. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K201859.

When did Porcine Mineral Collagen Composite Moldable receive FDA 510(k) clearance?

Porcine Mineral Collagen Composite Moldable received FDA 510(k) clearance on 2020-09-11, under 510(k) number K201859.

Who is the listed applicant for Porcine Mineral Collagen Composite Moldable?

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 Porcine Mineral Collagen Composite Moldable?

The FDA product code for Porcine Mineral Collagen Composite Moldable 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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