Reef L椎间系统;WaveForm L椎间系统
K号: K240566 · 2024-04-26
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器械摘要
常见问题
What is the Reef L Interbody System; WaveForm L Interbody System?
Reef L Interbody System; WaveForm L Interbody System is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is SeaSpine Orthopedics Corporation. The 510(k) number is K240566.
When did Reef L Interbody System; WaveForm L Interbody System receive FDA 510(k) clearance?
Reef L Interbody System; WaveForm L Interbody System received FDA 510(k) clearance on 2024-04-26, under 510(k) number K240566.
Who is the listed applicant for Reef L Interbody System; WaveForm L Interbody System?
The FDA 510(k) record lists SeaSpine Orthopedics Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reef L Interbody System; WaveForm L Interbody System?
The FDA product code for Reef L Interbody System; WaveForm L Interbody System is MAX.
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SeaSpine Orthopedics Corporation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:MAX)
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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