K243824
- 510(k) number
- K243824
- Device name
- Preat Abutments
- Applicant
- Preat Corporation CA · US
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-05-08
- Date received
- 2024-12-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K243824.pdf
Official FDA record: K243824
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.