K241753
- 510(k) number
- K241753
- Device name
- Immediate Molar Implants
- Applicant
- Biomet 3i, LLC FL · US
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-10-23
- Date received
- 2024-06-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K241753.pdf
Official FDA record: K241753
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.