PROPEL device— 510(k) K150392

Substantially Equivalent

Propel Orthodontics, LLC

FDA 510(k) clearance K150392 for PROPEL device, Substantially Equivalent on 2015-09-18. Applicant: Propel Orthodontics, LLC. Device class: 2.

Clearance details

Applicant: Propel Orthodontics, LLC
Product code: Code DZJ
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2015-02-18
Decision date: 2015-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milpitas, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.