FDA 510(k)

LINK® Embrace 肩关节系统 - 反向配置

K号: K212992 · 2021-11-18

决定日期2021-11-18

产品代码PHX

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

LINK® Embrace Shoulder System - Reverse Configuration is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 2021-11-18 under 510(k) number K212992. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LINK® Embrace Shoulder System - Reverse Configuration?

LINK® Embrace Shoulder System - Reverse Configuration is a medical device that received FDA 510(k) clearance on 2021-11-18. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K212992.

When did LINK® Embrace Shoulder System - Reverse Configuration receive FDA 510(k) clearance?

LINK® Embrace Shoulder System - Reverse Configuration received FDA 510(k) clearance on 2021-11-18, under 510(k) number K212992.

Who is the listed applicant for LINK® Embrace Shoulder System - Reverse Configuration?

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

What is the FDA product code for LINK® Embrace Shoulder System - Reverse Configuration?

The FDA product code for LINK® Embrace Shoulder System - Reverse Configuration is PHX.

列明Waldemar Link 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。

K261009MobileLink 髋臼杯系统 – 40mm ID 插件（多种）K250375Allure髋关节柄和髓内塞子 K243927MobileLink 髋臼杯系统 - 内部涂层 K241636MobileLink 髋臼杯系统 - 扩展线（多个）K231445LINK Embrace 肩关节系统 - 反向配置 K222066LINK MobileLink 髋臼杯系统

查看所有 30 个设备 →

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。