IMPLANT CENTER— 510(k) K072030

Substantially Equivalent

Satelec - Acteon Group

FDA 510(k) clearance K072030 for IMPLANT CENTER, Substantially Equivalent on 2007-11-19. Applicant: Satelec - Acteon Group. Device class: 2.

Clearance details

Applicant: Satelec - Acteon Group
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2007-07-24
Decision date: 2007-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Laurel, NJ, 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.