DeGen 医疗 Latitude-C AM 颈椎椎间盘融合系统
K号: K252737 · 2025-10-10
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器械摘要
常见问题
What is the DeGen Medical Latitude-C AM Cervical Interbody Fusion System?
DeGen Medical Latitude-C AM Cervical Interbody Fusion System is a medical device that received FDA 510(k) clearance on 2025-10-10. The listed applicant is Degen Medical. The 510(k) number is K252737.
When did DeGen Medical Latitude-C AM Cervical Interbody Fusion System receive FDA 510(k) clearance?
DeGen Medical Latitude-C AM Cervical Interbody Fusion System received FDA 510(k) clearance on 2025-10-10, under 510(k) number K252737.
Who is the listed applicant for DeGen Medical Latitude-C AM Cervical Interbody Fusion System?
The FDA 510(k) record lists Degen Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DeGen Medical Latitude-C AM Cervical Interbody Fusion System?
The FDA product code for DeGen Medical Latitude-C AM Cervical Interbody Fusion System is ODP.
相关临床试验
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列明Degen Medical为申报人的其他记录
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相关器械(代码:ODP)
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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