Renovis Tesera SC 独立式前颈椎融合(ACF)系统
K号: K153250 · 2016-03-16
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器械摘要
常见问题
What is the Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System?
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System is a medical device that received FDA 510(k) clearance on 2016-03-16. The listed applicant is Renovis Surgical Technologies. The 510(k) number is K153250.
When did Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System receive FDA 510(k) clearance?
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System received FDA 510(k) clearance on 2016-03-16, under 510(k) number K153250.
Who is the listed applicant for Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System?
The FDA 510(k) record lists Renovis Surgical Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System?
The FDA product code for Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System is OVE.
相关临床试验
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列明Renovis Surgical Technologies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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