Clearance Summary
Calibra Abutment Resin Cement received FDA 510(k) clearance under submission number K240888, sponsored by Dentsply Sirona. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-04-02.
- Submission: K240888
- Applicant / Sponsor: Dentsply Sirona
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3275
- Decision date: 2024-04-02
Classification & Regulation
This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.