K233806
- 510(k) number
- K233806
- Device name
- T2 Plus
- Applicant
- Osstem Implant Co., Ltd. KR
- Product code
- OAS — X-Ray, Tomography, Computed, Dental
- Decision date
- 2024-09-06
- Date received
- 2023-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233806.pdf
Official FDA record: K233806
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.