ELID(内镜下微创减压)系统
K号: K243774 · 2025-08-27
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器械摘要
常见问题
What is the ELID (Endoscopic Less Invasive Decompression) System?
ELID (Endoscopic Less Invasive Decompression) System is a medical device that received FDA 510(k) clearance on 2025-08-27. The listed applicant is Lesspine Innovations. The 510(k) number is K243774.
When did ELID (Endoscopic Less Invasive Decompression) System receive FDA 510(k) clearance?
ELID (Endoscopic Less Invasive Decompression) System received FDA 510(k) clearance on 2025-08-27, under 510(k) number K243774.
Who is the listed applicant for ELID (Endoscopic Less Invasive Decompression) System?
The FDA 510(k) record lists Lesspine Innovations as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELID (Endoscopic Less Invasive Decompression) System?
The FDA product code for ELID (Endoscopic Less Invasive Decompression) System is HRX.
相关临床试验
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列明Lesspine Innovations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。
相关器械(代码:HRX)
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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