K240888
- 510(k) number
- K240888
- Device name
- Calibra Abutment Resin Cement
- Applicant
- Dentsply Sirona PA · US
- Product code
- EMA — Cement, Dental
- Decision date
- 2024-04-02
- Date received
- 2024-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Flag
- Third-party review
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K240888.pdf
Official FDA record: K240888
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.