SPACER— 510(k) K072069

Substantially Equivalent

Vericom Co., Ltd.

FDA 510(k) clearance K072069 for SPACER, Substantially Equivalent on 2007-09-28. Applicant: Vericom Co., Ltd.. Device class: 2.

Clearance details

Applicant: Vericom Co., Ltd.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2007-07-30
Decision date: 2007-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mission Viejo, 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.