Auxilock 钛合金干扰螺钉
K号: K203029 · 2021-08-20
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器械摘要
常见问题
What is the Auxilock Titanium Interference Screw?
Auxilock Titanium Interference Screw is a medical device that received FDA 510(k) clearance on 2021-08-20. The listed applicant is Auxein Medical Private Limited. The 510(k) number is K203029.
When did Auxilock Titanium Interference Screw receive FDA 510(k) clearance?
Auxilock Titanium Interference Screw received FDA 510(k) clearance on 2021-08-20, under 510(k) number K203029.
Who is the listed applicant for Auxilock Titanium Interference Screw?
The FDA 510(k) record lists Auxein Medical Private Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Auxilock Titanium Interference Screw?
The FDA product code for Auxilock Titanium Interference Screw is HWC. This falls under the Cardiovascular category.
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。
列明Auxein Medical Private Limited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:HWC)
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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