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

ZIRCONIA IMPLANT

K Number: K061971 · Decision Mar 6, 2007
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
60
Review Days
237

Basic Information

Device Name
ZIRCONIA IMPLANT
K Number
K061971
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NOBEL BIOCARE AB
Date Received
July 12, 2006
Decision Date
March 6, 2007
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

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