Advantage-C™ Ti3D 颈椎椎间融合器
K号: K252711 · 2026-01-08
广告
器械摘要
常见问题
What is the Advantage-C™ Ti3D Cervical Interbody Fusion Device?
Advantage-C™ Ti3D Cervical Interbody Fusion Device is a medical device that received FDA 510(k) clearance on 2026-01-08. The listed applicant is Intelivation Technologies. The 510(k) number is K252711.
When did Advantage-C™ Ti3D Cervical Interbody Fusion Device receive FDA 510(k) clearance?
Advantage-C™ Ti3D Cervical Interbody Fusion Device received FDA 510(k) clearance on 2026-01-08, under 510(k) number K252711.
Who is the listed applicant for Advantage-C™ Ti3D Cervical Interbody Fusion Device?
The FDA 510(k) record lists Intelivation Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Advantage-C™ Ti3D Cervical Interbody Fusion Device?
The FDA product code for Advantage-C™ Ti3D Cervical Interbody Fusion Device is ODP.
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: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。
广告