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

HERO II DENTAL IMPLANT SYSTEM, UI DENTAL IMPLANT SYSTEM

K Number: K130221 · Decision Mar 21, 2013
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
51

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Basic Information

Device Name
HERO II DENTAL IMPLANT SYSTEM, UI DENTAL IMPLANT SYSTEM
K Number
K130221
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medimecca Co., Ltd.
Date Received
January 29, 2013
Decision Date
March 21, 2013
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 Medimecca Co., Ltd.

K Number Device Name
K202039 Honorst Implant System
K160536 Chaorum Implant System
K131682 UD IMPLANT SYSTEM