K211799 is an FDA 510(k) clearance for the Biodentine XP 500, Biodentine XP 200. This device is classified as a Resin, Root Canal Filling (Class II - Special Controls, product code KIF).
Submitted by Septodont (Saint-Maur Des Fosses Cedex, FR). The FDA issued a Cleared decision on August 10, 2021, 61 days after receiving the submission on June 10, 2021.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3820.
| 510(k) Number | K211799 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 10, 2021 |
| Decision Date | August 10, 2021 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | KIF - Resin, Root Canal Filling |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3820 |