FDA 510(k)

Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161

K号: K201072 · 2020-12-02

决定日期2020-12-02

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

Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161 is the device name listed in this FDA 510(k) record. The listed applicant is Ensemble Orthopedics, LLC. It received FDA 510(k) clearance on 2020-12-02 under 510(k) number K201072. 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 Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161?

Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161 is a medical device that received FDA 510(k) clearance on 2020-12-02. The listed applicant is Ensemble Orthopedics, LLC. The 510(k) number is K201072.

When did Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161 receive FDA 510(k) clearance?

Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161 received FDA 510(k) clearance on 2020-12-02, under 510(k) number K201072.

Who is the listed applicant for Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161?

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

What is the FDA product code for Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161?

The FDA product code for Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161 is KYI.

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。

Ensemble CMC, Size 141, Ensemble CMC, Size 151, Ensemble CMC, Size 161

器械摘要

常见问题

相关临床试验

相关器械（代码：KYI）

官方来源