FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS

K Number: K090081 · Decision Jun 22, 2010
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
3
Review Days
526

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Basic Information

Device Name
TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS
K Number
K090081
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Talladium Espana, SL
Date Received
January 12, 2009
Decision Date
June 22, 2010
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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K Number Device Name
K221966 Dynamic TiBase
K162021 3.0 Dynamic TiBase