FDA 510(k)

Comprehensive®可转换肩胛窝 - Vivacit-E衬里

K号: K211729 · 2021-11-04

决定日期2021-11-04

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

Comprehensive® Convertible Glenoid - Vivacit-E Liner is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2021-11-04 under 510(k) number K211729. 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 Comprehensive® Convertible Glenoid - Vivacit-E Liner?

Comprehensive® Convertible Glenoid - Vivacit-E Liner is a medical device that received FDA 510(k) clearance on 2021-11-04. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K211729.

When did Comprehensive® Convertible Glenoid - Vivacit-E Liner receive FDA 510(k) clearance?

Comprehensive® Convertible Glenoid - Vivacit-E Liner received FDA 510(k) clearance on 2021-11-04, under 510(k) number K211729.

Who is the listed applicant for Comprehensive® Convertible Glenoid - Vivacit-E Liner?

The FDA 510(k) record lists Biomet Manufacturing Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Comprehensive® Convertible Glenoid - Vivacit-E Liner?

The FDA product code for Comprehensive® Convertible Glenoid - Vivacit-E Liner is PHX.

列明Biomet Manufacturing Corp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。

K230540患者特异性规划解决方案™ 3D骨骼模型 K214001Comprehensive®肩关节系统，Comprehensive®反肩关节系统 K202232综合胸腔重建系统 K193038综合肩关节系统 K182516综合纳米无肩峰肩关节 K181611综合反向肩关节系统

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官方来源

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