Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System
K号: K240872 · 2024-04-26
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器械摘要
常见问题
What is the Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System?
Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is Clariance. The 510(k) number is K240872.
When did Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System receive FDA 510(k) clearance?
Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System received FDA 510(k) clearance on 2024-04-26, under 510(k) number K240872.
Who is the listed applicant for Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System?
The FDA 510(k) record lists Clariance as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System?
The FDA product code for Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System is NKB.
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。
列明Clariance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:NKB)
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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