Wishbone HA— 510(k) K211551

Substantially Equivalent

Wishbone SA

FDA 510(k) clearance K211551 for Wishbone HA, Substantially Equivalent on 2021-08-20. Applicant: Wishbone SA. Device class: 2.

Clearance details

Applicant: Wishbone SA
Product code: Code NPM
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2021-05-19
Decision date: 2021-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flemalle, BE

Download summary PDF View on FDA.gov ↗

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