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

ENDOSSEOUS DENTAL IMPLANT SYSTEM

K Number: K082651 · Decision Dec 22, 2008
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
5
Review Days
101

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Basic Information

Device Name
ENDOSSEOUS DENTAL IMPLANT SYSTEM
K Number
K082651
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Southern Implants, Inc.
Date Received
September 12, 2008
Decision Date
December 22, 2008
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

Similar 510(k) Clearances

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Other Clearances by Southern Implants, Inc.

K Number Device Name
K093562 ENDOSSEOUS DENTAL IMPLANT
K071161 ENDOSSEOUS DENTAL IMPLANT SYSTEM
K070841 ENDOSSEOUS DENTAL IMPLANT SYSTEM
K070905 ENDOSSEOUS DENTAL IMPLANT SYSTEM