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

CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS

K Number: K083496 · Decision Jan 30, 2009
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
14
Review Days
66

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Basic Information

Device Name
CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS
K Number
K083496
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Altatec GmbH
Date Received
November 25, 2008
Decision Date
January 30, 2009
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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Other Clearances by Altatec GmbH

K Number Device Name
K193401 Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants
K160784 CAM Titanium Blanks
K153779 Abutment for Bridges
K152509 CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)
K151599 iSy Implant System
K143337 CONELOG Titanium base CAD/CAM
K133991 ISY
K113779 CONELOG IMPLANT SYSTEM
K103252 CAMLOG VARIO SR ABUTMENTS
K090347 CAMLOG ABUTMENTS PS
Search all 14 clearances from Altatec GmbH →