EndoFix™ 组织固定系统
K号: K251229 · 2025-08-20
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器械摘要
常见问题
What is the EndoFix™Tissue Fixation System?
EndoFix™Tissue Fixation System is a medical device that received FDA 510(k) clearance on 2025-08-20. The listed applicant is Softac Medical Technologies. The 510(k) number is K251229.
When did EndoFix™Tissue Fixation System receive FDA 510(k) clearance?
EndoFix™Tissue Fixation System received FDA 510(k) clearance on 2025-08-20, under 510(k) number K251229.
Who is the listed applicant for EndoFix™Tissue Fixation System?
The FDA 510(k) record lists Softac Medical Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EndoFix™Tissue Fixation System?
The FDA product code for EndoFix™Tissue Fixation System is FGE.
相关临床试验
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相关器械(代码:FGE)
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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