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FDA 510(k)

Iatrical 内固定腰椎融合系统（ALIF型号，TLIF型号，LLIF型号）

K号: K232996 · 2024-09-06

申请人Shanghai Iatrical-Ti Technologies CO , Ltd.
决定日期2024-09-06
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

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Iatrical-Ti Technologies CO , Ltd.. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K232996. 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 Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)?

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Shanghai Iatrical-Ti Technologies CO , Ltd.. The 510(k) number is K232996.

When did Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) receive FDA 510(k) clearance?

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) received FDA 510(k) clearance on 2024-09-06, under 510(k) number K232996.

Who is the listed applicant for Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)?

The FDA 510(k) record lists Shanghai Iatrical-Ti Technologies CO , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)?

The FDA product code for Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) is MAX.

相关临床试验

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：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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