Submission Details
| 510(k) Number | K233252 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 28, 2023 |
| Decision Date | December 26, 2024 |
| Days to Decision | 455 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
K233252 is an FDA 510(k) clearance for the Straumann CARES Visual and Nova Dental CAD, a Dental Abutment Design Software For Dental Laboratory (Class II — Special Controls, product code PNP), submitted by Institut Straumann AG (Basel, CH). The FDA issued a Cleared decision on December 26, 2024, 455 days after receiving the submission on September 28, 2023. This device falls under the Dental review panel. Regulated under 21 CFR 872.3630.
| 510(k) Number | K233252 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 28, 2023 |
| Decision Date | December 26, 2024 |
| Days to Decision | 455 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | PNP — Dental Abutment Design Software For Dental Laboratory |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3630 |
| Definition | The Device Is Intended To Aid In The Restoration Of Chewing Function By Allowing A Dental Laboratory Or Dental Clinician To Design The Patient-specific Component Of A Dental Abutment (i.e. Abutment Collar And Abutment Post) And Cam Or Create That Component At A Dental Office Or Dental Laboratory Following The Directions Of The Dental Implant System. The Abutment-to-implant Interface/connection Platform Is Not A Patient-specific Component Of The Dental Abutment. |