K241616
- 510(k) number
- K241616
- Device name
- ALLONUS Tech Prosthetics
- Applicant
- Allonus Tech Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-12-17
- Date received
- 2024-06-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K241616.pdf
Official FDA record: K241616
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.