Momentum脊柱
K号: K232023 · 2023-10-04
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器械摘要
Momentum Spine is the device name listed in this FDA 510(k) record. The listed applicant is Momentum Health, Inc.. It received FDA 510(k) clearance on 2023-10-04 under 510(k) number K232023. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.
常见问题
What is the Momentum Spine?
Momentum Spine is a medical device that received FDA 510(k) clearance on 2023-10-04. The listed applicant is Momentum Health, Inc.. The 510(k) number is K232023.
When did Momentum Spine receive FDA 510(k) clearance?
Momentum Spine received FDA 510(k) clearance on 2023-10-04, under 510(k) number K232023.
Who is the listed applicant for Momentum Spine?
The FDA 510(k) record lists Momentum Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Momentum Spine?
The FDA product code for Momentum Spine is LDK.
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。
相关器械（代码：LDK）
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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