K231923
- 510(k) number
- K231923
- Device name
- Liberty SI Lateral Implant System
- Applicant
- Spinal Simplicity, LLC KS · US
- Product code
- OUR — Sacroiliac Joint Fixation
- Decision date
- 2023-12-05
- Date received
- 2023-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K231923.pdf
Official FDA record: K231923
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.