FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

BONEMEDIK-DM

K Number: K080772 · Decision Jun 3, 2008
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
21
Review Days
76

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Basic Information

Device Name
BONEMEDIK-DM
K Number
K080772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meta Biomed Co., Ltd.
Date Received
March 19, 2008
Decision Date
June 3, 2008
Product Code
LYC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYC Bone Grafting Material, Synthetic

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K191991 Ezfil
K190724 MD-Temp Plus
K190503 CeraSeal
K190510 GuttaSil
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