VMA™系统版本3.0
K号: K172327 · 2017-08-25
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器械摘要
VMA™ System version 3.0 is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Kinematics, Inc.. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K172327. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VMA™ System version 3.0?
VMA™ System version 3.0 is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is Ortho Kinematics, Inc.. The 510(k) number is K172327.
When did VMA™ System version 3.0 receive FDA 510(k) clearance?
VMA™ System version 3.0 received FDA 510(k) clearance on 2017-08-25, under 510(k) number K172327.
Who is the listed applicant for VMA™ System version 3.0?
The FDA 510(k) record lists Ortho Kinematics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VMA™ System version 3.0?
The FDA product code for VMA™ System version 3.0 is LLZ.
相关临床试验
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列明Ortho Kinematics, Inc.为申报人的其他记录
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相关器械（代码：LLZ）
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。
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官方来源
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