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

GC AADVA IMPLANT SYSTEM

K Number: K093749 · Decision Dec 6, 2010
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
127
Review Days
364

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Basic Information

Device Name
GC AADVA IMPLANT SYSTEM
K Number
K093749
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GC America, Inc.
Date Received
December 7, 2009
Decision Date
December 6, 2010
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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