NSite Scoliosis Assessment App— 510(k) K230463

Name: FDA 510(k) clearance K230463
Creator: U.S. Food and Drug Administration
Published: 2023-11-15

Substantially Equivalent

Nsite, Inc.

FDA 510(k) clearance K230463 for NSite Scoliosis Assessment App, Substantially Equivalent on 2023-11-15. Applicant: Nsite, Inc.. Device class: Unclassified.

Clearance details

Applicant: Nsite, Inc.
Product code: Code LDK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2023-02-21
Decision date: 2023-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

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