Assut Filbloc 永久缝合线
K号: K171039 · 2017-08-29
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决定日期2017-08-29
产品代码GAW
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
Assut Filbloc Permanent Sutures is the device name listed in this FDA 510(k) record. The listed applicant is Assut Europe S.P.A.. It received FDA 510(k) clearance on 2017-08-29 under 510(k) number K171039. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Assut Filbloc Permanent Sutures?
Assut Filbloc Permanent Sutures is a medical device that received FDA 510(k) clearance on 2017-08-29. The listed applicant is Assut Europe S.P.A.. The 510(k) number is K171039.
When did Assut Filbloc Permanent Sutures receive FDA 510(k) clearance?
Assut Filbloc Permanent Sutures received FDA 510(k) clearance on 2017-08-29, under 510(k) number K171039.
Who is the listed applicant for Assut Filbloc Permanent Sutures?
The FDA 510(k) record lists Assut Europe S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Assut Filbloc Permanent Sutures?
The FDA product code for Assut Filbloc Permanent Sutures is GAW.
相关临床试验
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相关器械（代码：GAW）
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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