K091023 is an FDA 510(k) clearance for the METAMORPHOSIS. This device is classified as a Material, Tooth Shade, Resin (Class II - Special Controls, product code EBF).
Submitted by Kerr Corporation (Orange, US). The FDA issued a Cleared decision on May 21, 2009, 41 days after receiving the submission on April 10, 2009.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.
| 510(k) Number | K091023 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 10, 2009 |
| Decision Date | May 21, 2009 |
| Days to Decision | 41 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EBF — Material, Tooth Shade, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3690 |