FDA 510(k)

CINA-CSpine

K号: K240942 · 2024-09-12

决定日期2024-09-12

产品代码QAS

咨询委员会RA

决定实质等同

器械摘要

CINA-CSpine is the device name listed in this FDA 510(k) record. The listed applicant is Avicenna.Ai. It received FDA 510(k) clearance on 2024-09-12 under 510(k) number K240942. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CINA-CSpine?

CINA-CSpine is a medical device that received FDA 510(k) clearance on 2024-09-12. The listed applicant is Avicenna.Ai. The 510(k) number is K240942.

When did CINA-CSpine receive FDA 510(k) clearance?

CINA-CSpine received FDA 510(k) clearance on 2024-09-12, under 510(k) number K240942.

Who is the listed applicant for CINA-CSpine?

The FDA 510(k) record lists Avicenna.Ai as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CINA-CSpine?

The FDA product code for CINA-CSpine is QAS.

列明Avicenna.Ai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。

K240612CINA-VCF K233342CINA-ASPECTS K233968CINA-iPE K221716CINA K210237CINA 胸部 K200855CINA

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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。