Thunderbolt™ 微创和Lancer™ 开放椎弓根螺钉系统
K号: K171456 · 2017-08-03
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器械摘要
常见问题
What is the Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems?
Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems is a medical device that received FDA 510(k) clearance on 2017-08-03. The listed applicant is Choicespine. The 510(k) number is K171456.
When did Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems receive FDA 510(k) clearance?
Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems received FDA 510(k) clearance on 2017-08-03, under 510(k) number K171456.
Who is the listed applicant for Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems?
The FDA 510(k) record lists Choicespine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems?
The FDA product code for Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems is NKB.
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Choicespine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:NKB)
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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