Submission Details
| 510(k) Number | K993505 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 15, 1999 |
| Decision Date | December 08, 1999 |
| Days to Decision | 54 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
K993505 is an FDA 510(k) clearance for the V-DELTA SPECIAL, ALLOY NO. 5154, a Alloy, Other Noble Metal (Class II — Special Controls, product code EJS), submitted by Metalor Dental USA Corp. (North Attleborough, US). The FDA issued a Cleared decision on December 8, 1999, 54 days after receiving the submission on October 15, 1999. This device falls under the Dental review panel. Regulated under 21 CFR 872.3060.
| 510(k) Number | K993505 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 15, 1999 |
| Decision Date | December 08, 1999 |
| Days to Decision | 54 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | EJS — Alloy, Other Noble Metal |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3060 |