FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OSBONE DENTAL

K Number: K102872 · Decision Jan 12, 2011
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
10
Review Days
104

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Basic Information

Device Name
OSBONE DENTAL
K Number
K102872
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Curasan AG
Date Received
September 30, 2010
Decision Date
January 12, 2011
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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Other Clearances by Curasan AG

K Number Device Name
K181721 Ceracell Ortho Foam
K160566 Cerasorb Ortho Foam
K111105 CURASAN OSSEOLIVE DENTAL
K103709 CERACELL DENTAL
K100841 BONEOPTIMIZER
K063106 REVOIS IMPLANT SYSTEM
K040216 CERASORB M ORTHO
K031651 MODIFICATION TO CERASORB ORTHO
K014156 CERASORB ORTHO