PROPEL Device— 510(k) K172164

Substantially Equivalent

Propel Orthodontics, LLC

FDA 510(k) clearance K172164 for PROPEL Device, Substantially Equivalent on 2018-01-17. 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: 2017-07-18
Decision date: 2018-01-17
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.