K193352 is an FDA 510(k) clearance for the AbutmentCAD. This device is classified as a Dental Abutment Design Software For Dental Laboratory (Class II - Special Controls, product code PNP).
Submitted by Exocad GmbH (Darmstadt, DE). The FDA issued a Cleared decision on July 21, 2021, 595 days after receiving the submission on December 4, 2019.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3630. 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..
| 510(k) Number | K193352 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 04, 2019 |
| Decision Date | July 21, 2021 |
| Days to Decision | 595 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. |