FDA 510(k)

Artus™颈椎板系统

K号: K202227 · 2020-09-14

决定日期2020-09-14

产品代码KWQ

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

Artus™ cervical plate system is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2020-09-14 under 510(k) number K202227. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Artus™ cervical plate system?

Artus™ cervical plate system is a medical device that received FDA 510(k) clearance on 2020-09-14. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K202227.

When did Artus™ cervical plate system receive FDA 510(k) clearance?

Artus™ cervical plate system received FDA 510(k) clearance on 2020-09-14, under 510(k) number K202227.

Who is the listed applicant for Artus™ cervical plate system?

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

What is the FDA product code for Artus™ cervical plate system?

The FDA product code for Artus™ cervical plate system is KWQ.

列明Ulrich 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。

K252281ulricheasyINJECT Max 2M（XD 10140）；ulricheasyINJECT Max 3（XD 10150）；ulricheasyINJECT Max 3（XD 10180）K251295ulrich注射CT运动（XD 8000）K241850ulricheasyINJECT Max 2M（XD 10140）；ulricheasyINJECT Max 3（XD 10150）；ulricheasyINJECT Max 3（XD 10180）K233737ulricheasyINJECT Max 2M（XD 10140）；ulricheasyINJECT Max 3（XD 10150）；ulricheasyINJECT Max 3（XD 10180）K210541ulrich注射CT运动 K192872ulrich注射CT运动

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官方来源

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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。