NuVasive® CoRoent® Small Interlock™ System
K号: K161442 · 2016-09-28
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器械摘要
常见问题
What is the NuVasive® CoRoent® Small Interlock™ System?
NuVasive® CoRoent® Small Interlock™ System is a medical device that received FDA 510(k) clearance on 2016-09-28. The listed applicant is Nu Vasive, Incorporated. The 510(k) number is K161442.
When did NuVasive® CoRoent® Small Interlock™ System receive FDA 510(k) clearance?
NuVasive® CoRoent® Small Interlock™ System received FDA 510(k) clearance on 2016-09-28, under 510(k) number K161442.
Who is the listed applicant for NuVasive® CoRoent® Small Interlock™ System?
The FDA 510(k) record lists Nu Vasive, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NuVasive® CoRoent® Small Interlock™ System?
The FDA product code for NuVasive® CoRoent® Small Interlock™ System is OVE.
相关临床试验
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列明Nu Vasive, Incorporated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:OVE)
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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