Stryker骨科髋部设备标签更新
K号: K243784 · 2025-02-06
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器械摘要
常见问题
What is the Stryker Orthopaedics Hip Devices Labeling Update?
Stryker Orthopaedics Hip Devices Labeling Update is a medical device that received FDA 510(k) clearance on 2025-02-06. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K243784.
When did Stryker Orthopaedics Hip Devices Labeling Update receive FDA 510(k) clearance?
Stryker Orthopaedics Hip Devices Labeling Update received FDA 510(k) clearance on 2025-02-06, under 510(k) number K243784.
Who is the listed applicant for Stryker Orthopaedics Hip Devices Labeling Update?
The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stryker Orthopaedics Hip Devices Labeling Update?
The FDA product code for Stryker Orthopaedics Hip Devices Labeling Update is LPH.
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Howmedica Osteonics Corp., Dba Stryker Orthopaedics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：LPH）
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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