K233563
- 510(k) number
- K233563
- Device name
- Navident
- Applicant
- Claronav, Inc. CA
- Product code
- PLV — Dental Stereotaxic Instrument
- Decision date
- 2024-07-25
- Date received
- 2023-11-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K233563.pdf
Official FDA record: K233563
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.