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FDA 510(k)

Spine Guidance 软件包（版本 5.1）；综合手术室设备（CORE）2 控制台；CORE Q 脚踏开关；PI Drive 2 电机；Elite Q 连接器和切割附件

K号: K241171 · 2024-07-25

申请人Stryker Leibinger GmbH & Co KG
决定日期2024-07-25
产品代码OLO
咨询委员会NE 请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同

器械摘要

Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger GmbH & Co KG. It received FDA 510(k) clearance on 2024-07-25 under 510(k) number K241171. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories?

Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories is a medical device that received FDA 510(k) clearance on 2024-07-25. The listed applicant is Stryker Leibinger GmbH & Co KG. The 510(k) number is K241171.

When did Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories receive FDA 510(k) clearance?

Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories received FDA 510(k) clearance on 2024-07-25, under 510(k) number K241171.

Who is the listed applicant for Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories?

The FDA 510(k) record lists Stryker Leibinger GmbH & Co KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories?

The FDA product code for Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories is OLO.

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Stryker Leibinger GmbH & Co KG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。

K261054肋板系统K254233MEDPOR 定制植入套件K253623Spine Guidance 5.4 软件包；Spine Guidance 5.4 升级；Spine Guidance 5.4 更新；Spine Guidance 5.4 软件启用；Spine Guidance 5.4 销售演示；Q 钻孔跟踪器；NavLock 适配器；Elite Q 连接器；Elite 切割附件；Maestro Air 电机K252871Spine Guidance 5.3 软件包；Q 内置体工具；Elite Q 连接器；Elite 切割附件K243491胸骨钢板扩张器K241517Q 导航系统；Mako 脊柱系统；

查看所有 19 个设备 →

相关器械（代码：OLO）

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。

K262506Remex脊柱外科导航 - 通用工具Remex Medical Corp.K261410Navbit MARQ（PRD-001-SUP（仰卧注册套件），PRD-001-LAT（侧卧注册套件））Suite 201, National Innovation CentreK261205SPINEART 导航仪器系统Spineart SAK261024TMINI微型机器人系统THINK Surgical, Inc.K262121离子-L 导航仪器SurGenTec, LLCK261113Op.n™ 脊柱导航和机器人引导Ecential Robotics

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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