Bony Trauma Extremity System (BTES) 螺钉范围,NX 钉
K号: K230118 · 2023-02-16
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器械摘要
常见问题
What is the Bony Trauma Extremity System (BTES) Screw Range, NX Nail?
Bony Trauma Extremity System (BTES) Screw Range, NX Nail is a medical device that received FDA 510(k) clearance on 2023-02-16. The listed applicant is Field Orthopaedics Pty, Ltd.. The 510(k) number is K230118.
When did Bony Trauma Extremity System (BTES) Screw Range, NX Nail receive FDA 510(k) clearance?
Bony Trauma Extremity System (BTES) Screw Range, NX Nail received FDA 510(k) clearance on 2023-02-16, under 510(k) number K230118.
Who is the listed applicant for Bony Trauma Extremity System (BTES) Screw Range, NX Nail?
The FDA 510(k) record lists Field Orthopaedics Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bony Trauma Extremity System (BTES) Screw Range, NX Nail?
The FDA product code for Bony Trauma Extremity System (BTES) Screw Range, NX Nail 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Field Orthopaedics Pty, Ltd.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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