免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据，仅供一般参考，不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

XCelliStem 创面粉

K号: K172593 · 2018-03-16

申请人Stemsys
决定日期2018-03-16
产品代码KGN
决定实质等同

器械摘要

XCelliStem Wound Powder is the device name listed in this FDA 510(k) record. The listed applicant is Stemsys. It received FDA 510(k) clearance on 2018-03-16 under 510(k) number K172593. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常见问题

What is the XCelliStem Wound Powder?

XCelliStem Wound Powder is a medical device that received FDA 510(k) clearance on 2018-03-16. The listed applicant is Stemsys. The 510(k) number is K172593.

When did XCelliStem Wound Powder receive FDA 510(k) clearance?

XCelliStem Wound Powder received FDA 510(k) clearance on 2018-03-16, under 510(k) number K172593.

Who is the listed applicant for XCelliStem Wound Powder?

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

What is the FDA product code for XCelliStem Wound Powder?

The FDA product code for XCelliStem Wound Powder 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

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。

↑