APTUS 肘部背侧尺骨鹰嘴板
K号: K240613 · 2024-06-20
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器械摘要
常见问题
What is the APTUS Elbow Dorsal Olecranon Plates?
APTUS Elbow Dorsal Olecranon Plates is a medical device that received FDA 510(k) clearance on 2024-06-20. The listed applicant is Medartis AG. The 510(k) number is K240613.
When did APTUS Elbow Dorsal Olecranon Plates receive FDA 510(k) clearance?
APTUS Elbow Dorsal Olecranon Plates received FDA 510(k) clearance on 2024-06-20, under 510(k) number K240613.
Who is the listed applicant for APTUS Elbow Dorsal Olecranon Plates?
The FDA 510(k) record lists Medartis AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APTUS Elbow Dorsal Olecranon Plates?
The FDA product code for APTUS Elbow Dorsal Olecranon Plates is HRS.
相关临床试验
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列明Medartis AG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:HRS)
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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