K230463
- 510(k) number
- K230463
- Device name
- NSite Scoliosis Assessment App
- Applicant
- Nsite, Inc. CA · US
- Product code
- LDK — Device, Sensing, Optical Contour
- Decision date
- 2023-11-15
- Date received
- 2023-02-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K230463.pdf
Official FDA record: K230463
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.