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FDA 510(k)

FaSet 固定系统，UNITY 骶髂关节固定系统，Huvex 间棘固定系统，以及 AEON-C™ 独立系统

K号: K232877 · 2023-12-13

申请人K&J Consulting Corporation
决定日期2023-12-13
产品代码MRW
决定实质等同

器械摘要

FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System is the device name listed in this FDA 510(k) record. The listed applicant is K&J Consulting Corporation. It received FDA 510(k) clearance on 2023-12-13 under 510(k) number K232877. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

常见问题

What is the FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System?

FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System is a medical device that received FDA 510(k) clearance on 2023-12-13. The listed applicant is K&J Consulting Corporation. The 510(k) number is K232877.

When did FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System receive FDA 510(k) clearance?

FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System received FDA 510(k) clearance on 2023-12-13, under 510(k) number K232877.

Who is the listed applicant for FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System?

The FDA 510(k) record lists K&J Consulting Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System?

The FDA product code for FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System is MRW.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明K&J Consulting Corporation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。

K212038K&J IVA（ACIF，DLIF，PLIF，TLIF，ALIF）PEEK笼

相关器械（代码：MRW）

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。

K262618Arthrex Spine Compression FT ScrewArthrex, Inc.K261209离子-LSurGenTec, LLCK253676CORUS® 后颈椎稳定系统 3D (CORUS® PCSS 3D)Providence Medical Technology, Inc.K253432DiversiVy® 关节突螺丝系统Vy Spine, LLCK251714离子-CSurGenTec, LLCK250679FFX Facet Fixation SystemSc Medica

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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