FDA 510(k)

ChoiceSpine Blackhawk Ti 颈椎间隙系统

K号: K203311 · 2021-05-10

决定日期2021-05-10

产品代码OVE

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

ChoiceSpine Blackhawk Ti Cervical Spacer System is the device name listed in this FDA 510(k) record. The listed applicant is Choice Spine, LLC. It received FDA 510(k) clearance on 2021-05-10 under 510(k) number K203311. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ChoiceSpine Blackhawk Ti Cervical Spacer System?

ChoiceSpine Blackhawk Ti Cervical Spacer System is a medical device that received FDA 510(k) clearance on 2021-05-10. The listed applicant is Choice Spine, LLC. The 510(k) number is K203311.

When did ChoiceSpine Blackhawk Ti Cervical Spacer System receive FDA 510(k) clearance?

ChoiceSpine Blackhawk Ti Cervical Spacer System received FDA 510(k) clearance on 2021-05-10, under 510(k) number K203311.

Who is the listed applicant for ChoiceSpine Blackhawk Ti Cervical Spacer System?

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

What is the FDA product code for ChoiceSpine Blackhawk Ti Cervical Spacer System?

The FDA product code for ChoiceSpine Blackhawk Ti Cervical Spacer System is OVE.

列明Choice Spine, 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。

K223869ChoiceSpine Blackhawk Ti 颈椎间隙系统 K220953ChoiceSpine TigerShark™ M，模块化椎间盘系统 K220024ChoiceSpine 导航系统 K211449特里顿™ 骶髂关节固定系统 K203561ChoiceSpine 导航系统 K201643ChoiceSpine Tiger Shark 颈椎间隙系统

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官方来源

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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。