K232049
- 510(k) number
- K232049
- Device name
- IS-III active Short Implant
- Applicant
- Neobiotech Co., Ltd. KR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-03-28
- Date received
- 2023-07-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K232049.pdf
Official FDA record: K232049
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.