Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring
PMA编号：P050018 · 2025-04-04
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决定日期2025-04-04
PMA 编号P050018
产品代码NWX
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]
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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
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring is the device name listed in this FDA 510(k) record. The listed applicant is Spectranetics Corp.. It received FDA 510(k) clearance on 2025-04-04. The device is classified under product code NWX. It was reviewed by the CV advisory panel.
常见问题
What is the Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring?
Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring is a medical device that received FDA 510(k) clearance on 2025-04-04. The listed applicant is Spectranetics Corp..
When did Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring receive FDA 510(k) clearance?
The clearance date for Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring can be found in the official FDA records.
谁是Catheter，经皮冠状动脉腔内成形术（PTCA），切割/打分产品的列名申请人？
The FDA 510(k) record lists Spectranetics Corp. as the applicant. This does not by itself establish the device manufacturer.
FDA导管、经皮腔内冠状动脉成形术（PTCA）、切割/打分产品的代码是什么？
FDA产品代码为Catheter，经皮腔内冠状动脉成形术（PTCA），切割/打分的是NWX。
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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