支架移植物，腓肠肌下，静脉动脉化
PMA编号：P220025 · 2026-01-07
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决定日期2026-01-07
PMA 编号P220025
产品代码QWN
设备分类第3类
医疗专科U
咨询委员会CV
请注意，由于原文未提供具体内容，以下是一个示例翻译：
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产品名称：[产品名称]
公司名称：[公司名称]
FDA批准号：[FDA批准号]
510(k)申请号：[510(k)申请号]
PMA申请号：[PMA申请号]
临床试验注册号：[NCT]
PubMed ID：[PMID]
产品标识符：[标识符]
产品URL：[URL]
---
请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
器械摘要
Stent graft, infrapopliteal, venous arterialization is the device name listed in this FDA 510(k) record. The listed applicant is LimFlow, Inc.. It received FDA 510(k) clearance on 2026-01-07. The device is classified under product code QWN. It was reviewed by the CV advisory panel.
常见问题
What is the Stent graft, infrapopliteal, venous arterialization?
Stent graft, infrapopliteal, venous arterialization is a medical device that received FDA 510(k) clearance on 2026-01-07. The listed applicant is LimFlow, Inc..
When did Stent graft, infrapopliteal, venous arterialization receive FDA 510(k) clearance?
The clearance date for Stent graft, infrapopliteal, venous arterialization can be found in the official FDA records.
Who is the listed applicant for Stent graft, infrapopliteal, venous arterialization?
The FDA 510(k) record lists LimFlow, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stent graft, infrapopliteal, venous arterialization?
The FDA product code for Stent graft, infrapopliteal, venous arterialization is QWN.
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。
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。
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