Trilor 盘片、块状物和拱形物
K号: K173643 · 2018-02-24
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决定日期2018-02-24
产品代码EBF
咨询委员会DE
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决定实质等同
器械摘要
Trilor Disks, Blocks and Arches is the device name listed in this FDA 510(k) record. The listed applicant is Bioloren S.R.L.. It received FDA 510(k) clearance on 2018-02-24 under 510(k) number K173643. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Trilor Disks, Blocks and Arches?
Trilor Disks, Blocks and Arches is a medical device that received FDA 510(k) clearance on 2018-02-24. The listed applicant is Bioloren S.R.L.. The 510(k) number is K173643.
When did Trilor Disks, Blocks and Arches receive FDA 510(k) clearance?
Trilor Disks, Blocks and Arches received FDA 510(k) clearance on 2018-02-24, under 510(k) number K173643.
Who is the listed applicant for Trilor Disks, Blocks and Arches?
The FDA 510(k) record lists Bioloren S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trilor Disks, Blocks and Arches?
The FDA product code for Trilor Disks, Blocks and Arches is EBF.
相关临床试验
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相关器械（代码：EBF）
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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