MedCAD AccuShape 钛合金患者特异性颅骨植入物
K号: K220357 · 2022-08-26
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器械摘要
常见问题
What is the MedCAD AccuShape Titanium Patient-Specific Cranial Implant?
MedCAD AccuShape Titanium Patient-Specific Cranial Implant is a medical device that received FDA 510(k) clearance on 2022-08-26. The listed applicant is Medcad. The 510(k) number is K220357.
When did MedCAD AccuShape Titanium Patient-Specific Cranial Implant receive FDA 510(k) clearance?
MedCAD AccuShape Titanium Patient-Specific Cranial Implant received FDA 510(k) clearance on 2022-08-26, under 510(k) number K220357.
Who is the listed applicant for MedCAD AccuShape Titanium Patient-Specific Cranial Implant?
The FDA 510(k) record lists Medcad as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MedCAD AccuShape Titanium Patient-Specific Cranial Implant?
The FDA product code for MedCAD AccuShape Titanium Patient-Specific Cranial Implant is GXN.
相关临床试验
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列明Medcad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：GXN）
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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