K233167
- 510(k) number
- K233167
- Device name
- LW Implant System Abutment
- Applicant
- Ossvis Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-03-25
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K233167.pdf
Official FDA record: K233167
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.