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

Ortho MI System

K Number: K211992 · Decision Oct 15, 2021
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
51
Applicant Total
20
Review Days
109

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Basic Information

Device Name
Ortho MI System
K Number
K211992
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteonic Co., Ltd.
Date Received
June 28, 2021
Decision Date
October 15, 2021
Product Code
OAT
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
OAT Implant, Endosseous, Orthodontic

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