K233805
- 510(k) number
- K233805
- Device name
- K5
- Applicant
- Osstem Implant Co., Ltd. Chair Business KR
- Product code
- EIA — Unit, Operative Dental
- Decision date
- 2024-09-03
- Date received
- 2023-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K233805.pdf
Official FDA record: K233805
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.