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

BR Type Implant System

K Number: K171179 · Decision Feb 9, 2018
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
6
Review Days
291

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Basic Information

Device Name
BR Type Implant System
K Number
K171179
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biotem Co., Ltd.
Date Received
April 24, 2017
Decision Date
February 9, 2018
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

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

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Other Clearances by Biotem Co., Ltd.

K Number Device Name
K222142 BR SLA Type Implant System
K222144 IR SLA Type Implant System
K190641 AR_N SLA Type Implant System
K171297 AR_N Type Implant System
K171185 IR Type Implant System