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

T1-CS, T1-C

K Number: K183475 · Decision Aug 30, 2019
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
68
Review Days
256

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Basic Information

Device Name
T1-CS, T1-C
K Number
K183475
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osstem Implant Co., Ltd.
Date Received
December 17, 2018
Decision Date
August 30, 2019
Product Code
OAS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OAS X-Ray, Tomography, Computed, Dental

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Other Clearances by Osstem Implant Co., Ltd.

K Number Device Name
K251434 Healing Abutment System
K251569 Bone Screw
K242521 Estar-ZE
K233806 T2 Plus
K233194 TS Abutment System
K232220 SS Abutment System
K232012 N1
K222778 Osstem Implant System
K221684 Osstem Abutment System
K212303 T2
Search all 68 clearances from Osstem Implant Co., Ltd. →