510(k) K230463 ยท LDK Device, Sensing, Optical Contour
NSite Scoliosis Assessment App
| Applicant | Nsite, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Nov 15, 2023 |
| Received | Feb 21, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230463
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.