CarboClear® X 椎弓根螺钉系统;CarboClear® X 导航仪器
K号: K233944 · 2024-01-10
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器械摘要
常见问题
What is the CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?
CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments is a medical device that received FDA 510(k) clearance on 2024-01-10. The listed applicant is CarboFix Orthopedics , Ltd.. The 510(k) number is K233944.
When did CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments receive FDA 510(k) clearance?
CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments received FDA 510(k) clearance on 2024-01-10, under 510(k) number K233944.
Who is the listed applicant for CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?
The FDA 510(k) record lists CarboFix Orthopedics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments?
The FDA product code for CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments 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CarboFix Orthopedics , Ltd.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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