膜螺丝和膜钉
K号: K201561 · 2020-10-05
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决定日期2020-10-05
产品代码DZL
咨询委员会DE
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决定实质等同
器械摘要
Membrane Screws and Membrane Tacks is the device name listed in this FDA 510(k) record. The listed applicant is Neoss Limited. It received FDA 510(k) clearance on 2020-10-05 under 510(k) number K201561. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Membrane Screws and Membrane Tacks?
Membrane Screws and Membrane Tacks is a medical device that received FDA 510(k) clearance on 2020-10-05. The listed applicant is Neoss Limited. The 510(k) number is K201561.
When did Membrane Screws and Membrane Tacks receive FDA 510(k) clearance?
Membrane Screws and Membrane Tacks received FDA 510(k) clearance on 2020-10-05, under 510(k) number K201561.
Who is the listed applicant for Membrane Screws and Membrane Tacks?
The FDA 510(k) record lists Neoss Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Membrane Screws and Membrane Tacks?
The FDA product code for Membrane Screws and Membrane Tacks is DZL.
相关临床试验
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：DZL）
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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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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