FDA 510(k)

全楔形侧向和增强基板

K号: K240278 · 2024-05-15

决定日期2024-05-15

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

Full Wedge Lateralized and Augmented Baseplates is the device name listed in this FDA 510(k) record. The listed applicant is Fx Shoulder USA, Inc.. It received FDA 510(k) clearance on 2024-05-15 under 510(k) number K240278. 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 Full Wedge Lateralized and Augmented Baseplates?

Full Wedge Lateralized and Augmented Baseplates is a medical device that received FDA 510(k) clearance on 2024-05-15. The listed applicant is Fx Shoulder USA, Inc.. The 510(k) number is K240278.

When did Full Wedge Lateralized and Augmented Baseplates receive FDA 510(k) clearance?

Full Wedge Lateralized and Augmented Baseplates received FDA 510(k) clearance on 2024-05-15, under 510(k) number K240278.

Who is the listed applicant for Full Wedge Lateralized and Augmented Baseplates?

The FDA 510(k) record lists Fx Shoulder USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Full Wedge Lateralized and Augmented Baseplates?

The FDA product code for Full Wedge Lateralized and Augmented Baseplates is PHX.

列明Fx Shoulder USA, Inc.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。

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官方来源

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