K100781 is an FDA 510(k) clearance for the OBSIDIAN CERAMIC BLOCKS. This device is classified as a Powder, Porcelain (Class II - Special Controls, product code EIH).
Submitted by Prismatik Dentalcraft, Inc. (Newport Beach, US). The FDA issued a Cleared decision on June 21, 2010, 94 days after receiving the submission on March 19, 2010.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6660.
| 510(k) Number | K100781 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 19, 2010 |
| Decision Date | June 21, 2010 |
| Days to Decision | 94 days |
| Submission Type | Abbreviated |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EIH — Powder, Porcelain |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.6660 |