Miromatrix 生物网 TW
K号: K162570 · 2017-02-16
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决定日期2017-02-16
产品代码FTM
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Miromatrix Biological Mesh TW is the device name listed in this FDA 510(k) record. The listed applicant is Miromatrix Medical, Inc.. It received FDA 510(k) clearance on 2017-02-16 under 510(k) number K162570. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Miromatrix Biological Mesh TW?
Miromatrix Biological Mesh TW is a medical device that received FDA 510(k) clearance on 2017-02-16. The listed applicant is Miromatrix Medical, Inc.. The 510(k) number is K162570.
When did Miromatrix Biological Mesh TW receive FDA 510(k) clearance?
Miromatrix Biological Mesh TW received FDA 510(k) clearance on 2017-02-16, under 510(k) number K162570.
Who is the listed applicant for Miromatrix Biological Mesh TW?
The FDA 510(k) record lists Miromatrix Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Miromatrix Biological Mesh TW?
The FDA product code for Miromatrix Biological Mesh TW is FTM.
相关临床试验
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列明Miromatrix Medical, 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。
相关器械（代码：FTM）
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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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