MINNE TIES MMF 缝线系统
K号: K162046 · 2017-04-11
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决定日期2017-04-11
产品代码DYX
咨询委员会DE
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决定实质等同
器械摘要
MINNE TIES MMF Suture System is the device name listed in this FDA 510(k) record. The listed applicant is Summit Medical, Inc.. It received FDA 510(k) clearance on 2017-04-11 under 510(k) number K162046. The device is classified under product code DYX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MINNE TIES MMF Suture System?
MINNE TIES MMF Suture System is a medical device that received FDA 510(k) clearance on 2017-04-11. The listed applicant is Summit Medical, Inc.. The 510(k) number is K162046.
When did MINNE TIES MMF Suture System receive FDA 510(k) clearance?
MINNE TIES MMF Suture System received FDA 510(k) clearance on 2017-04-11, under 510(k) number K162046.
Who is the listed applicant for MINNE TIES MMF Suture System?
The FDA 510(k) record lists Summit Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINNE TIES MMF Suture System?
The FDA product code for MINNE TIES MMF Suture System is DYX.
相关临床试验
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列明Summit 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。
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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