K232023
- 510(k) number
- K232023
- Device name
- Momentum Spine
- Applicant
- Momentum Health, Inc. CA
- Product code
- LDK — Device, Sensing, Optical Contour
- Decision date
- 2023-10-04
- Date received
- 2023-07-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
510(k) Summary (official FDA PDF): K232023.pdf
Official FDA record: K232023
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.