BONEMEDIK-DM— 510(k) K080772

Substantially Equivalent

Meta Biomed Co., Ltd.

FDA 510(k) clearance K080772 for BONEMEDIK-DM, Substantially Equivalent on 2008-06-03. Applicant: Meta Biomed Co., Ltd.. Device class: 2.

Clearance details

Applicant: Meta Biomed Co., Ltd.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2008-03-19
Decision date: 2008-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Republic Of Korea, KR

Download summary PDF View on FDA.gov ↗

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