FDA 510(k)

CAVUX 骨突固定系统（CAVUX FFS）和 CORUS-LX 移植

K号: K251885 · 2025-07-10

决定日期2025-07-10

产品代码MRW

决定实质等同

器械摘要

CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant is the device name listed in this FDA 510(k) record. The listed applicant is Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2025-07-10 under 510(k) number K251885. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

常见问题

What is the CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant?

CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant is a medical device that received FDA 510(k) clearance on 2025-07-10. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K251885.

When did CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant receive FDA 510(k) clearance?

CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant received FDA 510(k) clearance on 2025-07-10, under 510(k) number K251885.

Who is the listed applicant for CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant?

The FDA 510(k) record lists Providence Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant?

The FDA product code for CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant is MRW.

列明Providence Medical Technology, Inc.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。

K261665CORUS® 导航系统-GN K253676CORUS® 后颈椎稳定系统 3D (CORUS® PCSS 3D)K253190CORUS-LX 移植物 K251060CORUS® 导航系统-GX K241035PMT 后颈椎稳定系统（PCSS）K240625CORUS 导航访问系统

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