FDA 510(k)

猪无机骨矿物质递送应用器

K号: K162158 · 2017-02-09

决定日期2017-02-09

产品代码NPM

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决定实质等同

器械摘要

Porcine Anorganic Bone Mineral 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 2017-02-09 under 510(k) number K162158. 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 Anorganic Bone Mineral in Delivery Applicator?

Porcine Anorganic Bone Mineral in Delivery Applicator is a medical device that received FDA 510(k) clearance on 2017-02-09. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K162158.

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

Porcine Anorganic Bone Mineral in Delivery Applicator received FDA 510(k) clearance on 2017-02-09, under 510(k) number K162158.

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

The FDA product code for Porcine Anorganic Bone Mineral 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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