FDA 510(k)

uCerv Flux-C 3D多孔钛颈椎椎间植入物

K号: K220696 · 2022-08-19

决定日期2022-08-19

产品代码ODP

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

uCerv Flux-C 3D Porous Titanium Cervical Interbody is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich Medical USA. It received FDA 510(k) clearance on 2022-08-19 under 510(k) number K220696. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the uCerv Flux-C 3D Porous Titanium Cervical Interbody?

uCerv Flux-C 3D Porous Titanium Cervical Interbody is a medical device that received FDA 510(k) clearance on 2022-08-19. The listed applicant is Ulrich Medical USA. The 510(k) number is K220696.

When did uCerv Flux-C 3D Porous Titanium Cervical Interbody receive FDA 510(k) clearance?

uCerv Flux-C 3D Porous Titanium Cervical Interbody received FDA 510(k) clearance on 2022-08-19, under 510(k) number K220696.

Who is the listed applicant for uCerv Flux-C 3D Porous Titanium Cervical Interbody?

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

What is the FDA product code for uCerv Flux-C 3D Porous Titanium Cervical Interbody?

The FDA product code for uCerv Flux-C 3D Porous Titanium Cervical Interbody is ODP.

列明Ulrich Medical USA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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相关器械（代码：ODP）

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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