FDA 510(k)

综合节段性翻修系统(SRS)

K号: K223631 · 2023-07-12

决定日期2023-07-12

产品代码KWT

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 Segmental Revision System(SRS) is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics. It received FDA 510(k) clearance on 2023-07-12 under 510(k) number K223631. The device is classified under product code KWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Comprehensive Segmental Revision System(SRS)?

Comprehensive Segmental Revision System(SRS) is a medical device that received FDA 510(k) clearance on 2023-07-12. The listed applicant is Biomet Orthopedics. The 510(k) number is K223631.

When did Comprehensive Segmental Revision System(SRS) receive FDA 510(k) clearance?

Comprehensive Segmental Revision System(SRS) received FDA 510(k) clearance on 2023-07-12, under 510(k) number K223631.

Who is the listed applicant for Comprehensive Segmental Revision System(SRS)?

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

What is the FDA product code for Comprehensive Segmental Revision System(SRS)?

The FDA product code for Comprehensive Segmental Revision System(SRS) is KWT.

列明Biomet Orthopedics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。

K252404综合反向肩关节 - HA股骨头底板 K243761A.L.P.S. 小骨片钢板系统 K200196Taperloc® 完整髋臼柄

官方来源

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