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

ORTHODONTIC SCREW

K Number: K103105 · Decision Mar 25, 2011
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
51
Applicant Total
68
Review Days
156

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Basic Information

Device Name
ORTHODONTIC SCREW
K Number
K103105
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osstem Implant Co., Ltd.
Date Received
October 20, 2010
Decision Date
March 25, 2011
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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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. →