Materialise肩关节系统™,Materialise肩关节引导和模型,SurgiCase肩关节规划器
K号: K242813 · 2024-10-18
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器械摘要
常见问题
What is the Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner?
Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner is a medical device that received FDA 510(k) clearance on 2024-10-18. The listed applicant is Materialise NV. The 510(k) number is K242813.
When did Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner receive FDA 510(k) clearance?
Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner received FDA 510(k) clearance on 2024-10-18, under 510(k) number K242813.
Who is the listed applicant for Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner?
The FDA 510(k) record lists Materialise NV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner?
The FDA product code for Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner is QHE.
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Materialise NV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:QHE)
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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