Spine CAMP™ (1.1)
K号: K231668 · 2023-07-07
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器械摘要
Spine CAMP™ (1.1) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Metrics, Inc.. It received FDA 510(k) clearance on 2023-07-07 under 510(k) number K231668. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Spine CAMP™ (1.1)?
Spine CAMP™ (1.1) is a medical device that received FDA 510(k) clearance on 2023-07-07. The listed applicant is Medical Metrics, Inc.. The 510(k) number is K231668.
When did Spine CAMP™ (1.1) receive FDA 510(k) clearance?
Spine CAMP™ (1.1) received FDA 510(k) clearance on 2023-07-07, under 510(k) number K231668.
Who is the listed applicant for Spine CAMP™ (1.1)?
The FDA 510(k) record lists Medical Metrics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spine CAMP™ (1.1)?
The FDA product code for Spine CAMP™ (1.1) is QIH.
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Medical Metrics, 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：QIH）
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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