NSite Scoliosis Assessment App
K-Number: K230463 · 2023-11-15
Device Summary
NSite Scoliosis Assessment App is a medical device manufactured by Nsite, Inc.. It received FDA 510(k) clearance on 2023-11-15 under approval number K230463. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
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. It is manufactured by Nsite, Inc.. The 510(k) number is K230463.
When was NSite Scoliosis Assessment App approved by the FDA?
NSite Scoliosis Assessment App received FDA 510(k) clearance on 2023-11-15, under approval number K230463.
What company makes NSite Scoliosis Assessment App?
NSite Scoliosis Assessment App is manufactured by Nsite, Inc..
What is the FDA product code for NSite Scoliosis Assessment App?
The FDA product code for NSite Scoliosis Assessment App is LDK.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.