Kyphon HV-R Bone Cement
K号: K160983 · 2016-08-24
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器械摘要
Kyphon HV-R Bone Cement is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2016-08-24 under 510(k) number K160983. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Kyphon HV-R Bone Cement?
Kyphon HV-R Bone Cement is a medical device that received FDA 510(k) clearance on 2016-08-24. The listed applicant is Medtronic, Inc.. The 510(k) number is K160983.
When did Kyphon HV-R Bone Cement receive FDA 510(k) clearance?
Kyphon HV-R Bone Cement received FDA 510(k) clearance on 2016-08-24, under 510(k) number K160983.
Who is the listed applicant for Kyphon HV-R Bone Cement?
The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kyphon HV-R Bone Cement?
The FDA product code for Kyphon HV-R Bone Cement is NDN.
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列明Medtronic, 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。
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相关器械（代码：NDN）
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。
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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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