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FDA 510(k)

锁定板和螺钉系统

K号: K240958 · 2025-02-10

申请人Hebei Ruihe Medical Devices Co., Ltd.
决定日期2025-02-10
产品代码HRS
咨询委员会OR 请注意，由于原文中未提供具体的医疗设备监管文本，以下是一个示例翻译，您可以根据实际文本进行调整： --- 产品名称：[产品名称] 公司名称：[公司名称] 根据FDA 510(k)预市场批准程序，[产品名称]已获得批准，用于[产品用途描述]。 产品注册号：[注册号] PMA编号：[PMA编号] 临床试验编号（NCT）：[NCT编号] PubMed ID（PMID）：[PMID编号] 更多信息请访问以下链接： [URL] --- 请将上述示例中的[产品名称]、[公司名称]、[注册号]、[PMA编号]、[NCT编号]、[PMID编号]和[URL]替换为实际的文本内容。
决定实质等同

器械摘要

Locking Plates and Screws Systems is the device name listed in this FDA 510(k) record. The listed applicant is Hebei Ruihe Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2025-02-10 under 510(k) number K240958. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Locking Plates and Screws Systems?

Locking Plates and Screws Systems is a medical device that received FDA 510(k) clearance on 2025-02-10. The listed applicant is Hebei Ruihe Medical Devices Co., Ltd.. The 510(k) number is K240958.

When did Locking Plates and Screws Systems receive FDA 510(k) clearance?

Locking Plates and Screws Systems received FDA 510(k) clearance on 2025-02-10, under 510(k) number K240958.

Who is the listed applicant for Locking Plates and Screws Systems?

The FDA 510(k) record lists Hebei Ruihe Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Locking Plates and Screws Systems?

The FDA product code for Locking Plates and Screws Systems is HRS.

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

相关器械（代码：HRS）

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。

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官方来源

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