FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Magicore II System

K Number: K201621 · Decision Jul 15, 2020
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
15
Review Days
30

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Basic Information

Device Name
Magicore II System
K Number
K201621
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innobiosurg Co., Ltd.
Date Received
June 15, 2020
Decision Date
July 15, 2020
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 Innobiosurg Co., Ltd.

K Number Device Name
K220517 IBS System
K220079 Magicore Narrow System
K212517 Magicore System
K203344 Premilled Titanium Block System
K202418 Magic UCLA Abutment System
K202479 IBS Implant System
K201981 Magicore System
K200753 IBS Implant System II
K192197 Magicore II System
K173120 CCM Abutment System
Search all 15 clearances from Innobiosurg Co., Ltd. →