FDA 510(k)

EquivaBone 骨诱导骨移植替代品 (EquivaBone )

K号: K243609 · 2024-12-18

决定日期2024-12-18

产品代码MQV

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

EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) is the device name listed in this FDA 510(k) record. The listed applicant is Etex Corporation. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K243609. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )?

EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Etex Corporation. The 510(k) number is K243609.

When did EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) receive FDA 510(k) clearance?

EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) received FDA 510(k) clearance on 2024-12-18, under 510(k) number K243609.

Who is the listed applicant for EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )?

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

What is the FDA product code for EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )?

The FDA product code for EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) is MQV.

列明Etex Corporation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。

K182107CarriGen PF

相关器械（代码：MQV）

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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