FDA 510(k)

可扩张腰椎融合笼（类型 I，类型 II）

K号: K232069 · 2023-11-29

申请人Shanghai Reach Medical Instrument Co, Ltd.

决定日期2023-11-29

产品代码MAX

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

Expandable Lumbar Fusion Cage (Type I,Type II) is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Reach Medical Instrument Co, Ltd.. It received FDA 510(k) clearance on 2023-11-29 under 510(k) number K232069. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Expandable Lumbar Fusion Cage (Type I,Type II)?

Expandable Lumbar Fusion Cage (Type I,Type II) is a medical device that received FDA 510(k) clearance on 2023-11-29. The listed applicant is Shanghai Reach Medical Instrument Co, Ltd.. The 510(k) number is K232069.

When did Expandable Lumbar Fusion Cage (Type I,Type II) receive FDA 510(k) clearance?

Expandable Lumbar Fusion Cage (Type I,Type II) received FDA 510(k) clearance on 2023-11-29, under 510(k) number K232069.

Who is the listed applicant for Expandable Lumbar Fusion Cage (Type I,Type II)?

The FDA 510(k) record lists Shanghai Reach Medical Instrument Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Expandable Lumbar Fusion Cage (Type I,Type II)?

The FDA product code for Expandable Lumbar Fusion Cage (Type I,Type II) is MAX.

列明Shanghai Reach Medical Instrument Co, Ltd.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。

K221745无菌后路脊柱固定系统 K201737后路脊柱固定系统

相关器械（代码：MAX）

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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官方来源

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