FDA 510(k)

Stablyx CMC 关节置换植入系统

K号: K180744 · 2018-04-11

决定日期2018-04-11

产品代码KYI

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

Stablyx CMC Arthroplasty Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Skeletal Dynamics, LLC. It received FDA 510(k) clearance on 2018-04-11 under 510(k) number K180744. The device is classified under product code KYI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Stablyx CMC Arthroplasty Implant System?

Stablyx CMC Arthroplasty Implant System is a medical device that received FDA 510(k) clearance on 2018-04-11. The listed applicant is Skeletal Dynamics, LLC. The 510(k) number is K180744.

When did Stablyx CMC Arthroplasty Implant System receive FDA 510(k) clearance?

Stablyx CMC Arthroplasty Implant System received FDA 510(k) clearance on 2018-04-11, under 510(k) number K180744.

Who is the listed applicant for Stablyx CMC Arthroplasty Implant System?

The FDA 510(k) record lists Skeletal Dynamics, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stablyx CMC Arthroplasty Implant System?

The FDA product code for Stablyx CMC Arthroplasty Implant System is KYI.

列明Skeletal Dynamics, LLC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。

K182492Geminus 腕骨远端板系统 K172688Align桡骨头系统 K171590远端肘部钢板系统

官方来源

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