FDA 510(k)

Osprey 缝线锚

K号: K243726 · 2025-01-30

决定日期2025-01-30

产品代码MBI

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

Osprey Suture Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Responsive Arthroscopy, Inc.. It received FDA 510(k) clearance on 2025-01-30 under 510(k) number K243726. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Osprey Suture Anchor?

Osprey Suture Anchor is a medical device that received FDA 510(k) clearance on 2025-01-30. The listed applicant is Responsive Arthroscopy, Inc.. The 510(k) number is K243726.

When did Osprey Suture Anchor receive FDA 510(k) clearance?

Osprey Suture Anchor received FDA 510(k) clearance on 2025-01-30, under 510(k) number K243726.

Who is the listed applicant for Osprey Suture Anchor?

FDA 510(k)记录将Responsive Arthroscopy, Inc.列为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Osprey Suture Anchor?

The FDA product code for Osprey Suture Anchor is MBI.

列明Responsive Arthroscopy, Inc.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。

K261632雷霆系统

官方来源

在 FDA 数据库中查看 →

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。