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FDA 510(k)

FiberLocker系统：FiberLocker植入物（SpeedPatch PET），FiberLocker仪器（FiberLocker仪器SN）

K号: K241219 · 2024-12-11

申请人ZuriMED Technologies AG
决定日期2024-12-11
产品代码OWX
咨询委员会SU 请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) is the device name listed in this FDA 510(k) record. The listed applicant is ZuriMED Technologies AG. It received FDA 510(k) clearance on 2024-12-11 under 510(k) number K241219. The device is classified under product code OWX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN)?

FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) is a medical device that received FDA 510(k) clearance on 2024-12-11. The listed applicant is ZuriMED Technologies AG. The 510(k) number is K241219.

When did FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) receive FDA 510(k) clearance?

FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) received FDA 510(k) clearance on 2024-12-11, under 510(k) number K241219.

Who is the listed applicant for FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN)?

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

What is the FDA product code for FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN)?

The FDA product code for FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) is OWX.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明ZuriMED Technologies AG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。

K253867FiberLocker植入物；FiberLocker仪器；FiberLocker动力单元

相关器械（代码：OWX）

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。

K253867FiberLocker植入物；FiberLocker仪器；FiberLocker动力单元ZuriMED Technologies AGK250997Integrity™ ImplantAnika Therapeutics, Inc.K243480SuturePatch组织加固Arthrex, Inc.K223538Integrity ImplantAnika Therapeutics, Inc.

官方来源

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