OsteoCentric骨板和螺钉系统
K号: K250494 · 2025-03-18
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器械摘要
常见问题
What is the The OsteoCentric Bone Plate and Screw System?
The OsteoCentric Bone Plate and Screw System is a medical device that received FDA 510(k) clearance on 2025-03-18. The listed applicant is OsteoCentric Technologies. The 510(k) number is K250494.
When did The OsteoCentric Bone Plate and Screw System receive FDA 510(k) clearance?
The OsteoCentric Bone Plate and Screw System received FDA 510(k) clearance on 2025-03-18, under 510(k) number K250494.
Who is the listed applicant for The OsteoCentric Bone Plate and Screw System?
The FDA 510(k) record lists OsteoCentric Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for The OsteoCentric Bone Plate and Screw System?
The FDA product code for The OsteoCentric Bone Plate and Screw System is HRS.
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OsteoCentric Technologies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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