Vitoss 双模态骨移植替代泡沫条
K号: K153608 · 2016-02-12
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器械摘要
常见问题
What is the Vitoss BiModal Bone Graft Substitute Foam Strip?
Vitoss BiModal Bone Graft Substitute Foam Strip is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Orthovita, Inc.. The 510(k) number is K153608.
When did Vitoss BiModal Bone Graft Substitute Foam Strip receive FDA 510(k) clearance?
Vitoss BiModal Bone Graft Substitute Foam Strip received FDA 510(k) clearance on 2016-02-12, under 510(k) number K153608.
Who is the listed applicant for Vitoss BiModal Bone Graft Substitute Foam Strip?
The FDA 510(k) record lists Orthovita, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vitoss BiModal Bone Graft Substitute Foam Strip?
The FDA product code for Vitoss BiModal Bone Graft Substitute Foam Strip is MQV.
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Orthovita, 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:MQV)
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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