Camber 脊柱技术 SPIRA - V® 开放矩阵椎体切除术笼
K号: K173800 · 2018-02-02
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器械摘要
常见问题
What is the Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage?
Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage is a medical device that received FDA 510(k) clearance on 2018-02-02. The listed applicant is Camber Spine Technologies. The 510(k) number is K173800.
When did Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage receive FDA 510(k) clearance?
Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage received FDA 510(k) clearance on 2018-02-02, under 510(k) number K173800.
Who is the listed applicant for Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage?
The FDA 510(k) record lists Camber Spine Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage?
The FDA product code for Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage is MQP.
相关临床试验
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。
列明Camber Spine 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:MQP)
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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