K233706
- 510(k) number
- K233706
- Device name
- Bendini Cloud Application
- Applicant
- Nuvasive CA · US
- Product code
- OLO — Orthopedic Stereotaxic Instrument
- Decision date
- 2024-08-02
- Date received
- 2023-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K233706.pdf
Official FDA record: K233706
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.