Intellijoint HIP 系统（车用），Intellijoint HIP 系统（便携式），Intellijoint HIP 仪器托盘
K号: K171525 · 2017-10-30
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决定日期2017-10-30
产品代码OLO
咨询委员会NE
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决定实质等同
器械摘要
Intellijoint HIP Generation 2B System is the device name listed in this FDA 510(k) record. The listed applicant is Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2017-10-30 under 510(k) number K171525. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Intellijoint HIP Generation 2B System?
Intellijoint HIP Generation 2B System is a medical device that received FDA 510(k) clearance on 2017-10-30. The listed applicant is Intellijoint Surgical, Inc.. The 510(k) number is K171525.
When did Intellijoint HIP Generation 2B System receive FDA 510(k) clearance?
Intellijoint HIP Generation 2B System received FDA 510(k) clearance on 2017-10-30, under 510(k) number K171525.
Who is the listed applicant for Intellijoint HIP Generation 2B System?
The FDA 510(k) record lists Intellijoint Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intellijoint HIP Generation 2B System?
The FDA product code for Intellijoint HIP Generation 2B System is OLO.
相关临床试验
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列明Intellijoint Surgical, 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：OLO）
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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