NSite脊柱侧弯评估应用
K号: K230463 · 2023-11-15
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器械摘要
NSite Scoliosis Assessment App is the device name listed in this FDA 510(k) record. The listed applicant is Nsite, Inc.. It received FDA 510(k) clearance on 2023-11-15 under 510(k) number K230463. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.
常见问题
What is the NSite Scoliosis Assessment App?
NSite Scoliosis Assessment App is a medical device that received FDA 510(k) clearance on 2023-11-15. The listed applicant is Nsite, Inc.. The 510(k) number is K230463.
When did NSite Scoliosis Assessment App receive FDA 510(k) clearance?
NSite Scoliosis Assessment App received FDA 510(k) clearance on 2023-11-15, under 510(k) number K230463.
Who is the listed applicant for NSite Scoliosis Assessment App?
The FDA 510(k) record lists Nsite, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NSite Scoliosis Assessment App?
The FDA product code for NSite Scoliosis Assessment App is LDK.
相关临床试验
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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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