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FDA 510(k)

InnovaMatrix®FD

K号: K241866 · 2024-07-26

申请人Convatec Triad Life Sciences, LLC
决定日期2024-07-26
产品代码KGN
决定实质等同

器械摘要

InnovaMatrix®FD is the device name listed in this FDA 510(k) record. The listed applicant is Convatec Triad Life Sciences, LLC. It received FDA 510(k) clearance on 2024-07-26 under 510(k) number K241866. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常见问题

What is the InnovaMatrix®FD?

InnovaMatrix®FD is a medical device that received FDA 510(k) clearance on 2024-07-26. The listed applicant is Convatec Triad Life Sciences, LLC. The 510(k) number is K241866.

When did InnovaMatrix®FD receive FDA 510(k) clearance?

InnovaMatrix®FD received FDA 510(k) clearance on 2024-07-26, under 510(k) number K241866.

Who is the listed applicant for InnovaMatrix®FD?

The FDA 510(k) record lists Convatec Triad Life Sciences, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InnovaMatrix®FD?

The FDA product code for InnovaMatrix®FD is KGN.

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

相关器械（代码：KGN）

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。

K260652ColActive PlusCovalon Technologies, Ltd.K260711Accelagen Plus 手术基质，1cc（CG-01AP）；Accelagen Plus 手术基质，3cc（CG-03AP）；Accelagen Plus 手术基质，5cc（CG-05AP）；Accelagen Plus 手术条带，125x25x2mm（CG-125X25AP）；Accelagen Plus 手术条带，250x25x2mm（CG-250X25AP）Berkeley Advanced BiomaterialsK260596胶原蛋白伤口粉Ventris MedicalK260669Endoform 皮肤模板Aroa Biosurgery , Ltd.K253521ECMT-100 WMDEcm Therapeutics, Inc.K253204CatalyzeBioTissue Holdings, Inc.

官方来源

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