BENDA WEDGE— 510(k) K140144

Substantially Equivalent

Centrix, Inc.

FDA 510(k) clearance K140144 for BENDA WEDGE, Substantially Equivalent on 2014-07-08. Applicant: Centrix, Inc.. Device class: 1.

Clearance details

Applicant: Centrix, Inc.
Product code: Code EJB
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 2014-01-22
Decision date: 2014-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shelton, CT, 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.