外科规划软件版本 1.1
K号: K173247 · 2017-11-08
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器械摘要
Surgical Planning Software version 1.1 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 2017-11-08 under 510(k) number K173247. 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 Surgical Planning Software version 1.1?
Surgical Planning Software version 1.1 is a medical device that received FDA 510(k) clearance on 2017-11-08. The listed applicant is Ortho Kinematics, Inc.. The 510(k) number is K173247.
When did Surgical Planning Software version 1.1 receive FDA 510(k) clearance?
Surgical Planning Software version 1.1 received FDA 510(k) clearance on 2017-11-08, under 510(k) number K173247.
Who is the listed applicant for Surgical Planning Software version 1.1?
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 Surgical Planning Software version 1.1?
The FDA product code for Surgical Planning Software version 1.1 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
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：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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