K240966
- 510(k) number
- K240966
- Device name
- Prima Plus Conical Implant System
- Applicant
- Keystone Dental, Inc. MA · US
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-07-09
- Date received
- 2024-04-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K240966.pdf
Official FDA record: K240966
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.