PROPEL Device— 510(k) K172164
Substantially EquivalentPropel Orthodontics, LLC
FDA 510(k) clearance K172164 for PROPEL Device, Substantially Equivalent on 2018-01-17. Applicant: Propel Orthodontics, LLC.
Clearance details
- Applicant
- Propel Orthodontics, LLC
- Product code
- Code DZJ
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milpitas, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.