K232220
- 510(k) number
- K232220
- Device name
- SS Abutment System
- Applicant
- Osstem Implant Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2023-12-05
- Date received
- 2023-07-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K232220.pdf
Official FDA record: K232220
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.