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

CMI IMPLANT IS SYSTEM

K Number: K113554 · Decision Apr 5, 2012
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
17
Review Days
126

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Basic Information

Device Name
CMI IMPLANT IS SYSTEM
K Number
K113554
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neobiotech Co., Ltd.
Date Received
December 1, 2011
Decision Date
April 5, 2012
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 Neobiotech Co., Ltd.

K Number Device Name
K232528 Protective Cap
K232049 IS-III active Short Implant
K210903 IS Multi Unit Abutment System
K190849 IS-III active System_S-narrow Type
K181137 IT-III active System
K181138 IS-III active System
K181178 S-mini active Fixture
K173938 IS-III HActive Fixture
K160991 Neo GBR System
K120503 CMI IMPLANT IS II ACTIVE
Search all 17 clearances from Neobiotech Co., Ltd. →