FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
T2
K Number: K212303
·
Decision Sep 21, 2021
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
68
Review Days
60
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Basic Information
- Device Name
- T2
- K Number
- K212303
- 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
- July 23, 2021
- Decision Date
- September 21, 2021
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| OAS | X-Ray, Tomography, Computed, Dental | FDA class 2 | Radiology |
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Other Clearances by Osstem Implant Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K251434 | Healing Abutment System | Mar 4, 2026 | Substantially Equivalent |
| K251569 | Bone Screw | Aug 13, 2025 | Substantially Equivalent |
| K242521 | Estar-ZE | Nov 20, 2024 | Substantially Equivalent |
| K233806 | T2 Plus | Sep 6, 2024 | Substantially Equivalent |
| K233194 | TS Abutment System | Feb 20, 2024 | Substantially Equivalent |
| K232220 | SS Abutment System | Dec 5, 2023 | Substantially Equivalent |
| K232012 | N1 | Nov 28, 2023 | Substantially Equivalent |
| K222778 | Osstem Implant System | Sep 23, 2023 | Substantially Equivalent |
| K221684 | Osstem Abutment System | Sep 8, 2022 | Substantially Equivalent |
| K210097 | Estar-Z | Jul 2, 2021 | Substantially Equivalent |