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

ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE

K Number: K063734 · Decision Mar 2, 2007
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
18
Review Days
74

Basic Information

Device Name
ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE
K Number
K063734
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ATLANTIS COMPONENTS, INC.
Date Received
December 18, 2006
Decision Date
March 2, 2007
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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Other Clearances by ATLANTIS COMPONENTS, INC.

K Number Device Name
K103020 ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT
K073540 ATLANTIS ABUTMENT IN ZIRCONIA FOR BIOHORIZONS IMPLANT
K073258 ATLANTIS ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI + ABUTMENT
K072483 ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI ABUTMENT IN ZIRCONIA FOR ASTRA IMPLANTS
K071946 ATLANTIS, GEMINI AND GEMINI+ ABUTMENTS IN ZIRCONIA FOR ASTRA IMPLANTS
K070833 ATLANTIS ABUTMENT FOR ASTRA IMPLANT
K062197 ATLANTIS ABUTMENT FOR 3I CERTAIN MICRO MINI; GEMINI AND GEMINI+ ABUTMENT
K062069 ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT
K062277 ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE
K053654 ATLANTIS ABUTMENT FOR NOBEL REPLACE INTERFACE
Search all 18 clearances from ATLANTIS COMPONENTS, INC. →