PeriPRO™ 股骨系统,可变角度固定系统,AxSOS 3Ti,Stryker 板系统
K号: K222381 · 2023-04-27
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器械摘要
常见问题
What is the PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System?
PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System is a medical device that received FDA 510(k) clearance on 2023-04-27. The listed applicant is Stryker GmbH. The 510(k) number is K222381.
When did PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System receive FDA 510(k) clearance?
PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System received FDA 510(k) clearance on 2023-04-27, under 510(k) number K222381.
Who is the listed applicant for PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System?
The FDA 510(k) record lists Stryker GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System?
The FDA product code for PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating 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Stryker GmbH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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