Submission Details
| 510(k) Number | K040524 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 01, 2004 |
| Decision Date | May 20, 2004 |
| Days to Decision | 80 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
K040524 is an FDA 510(k) clearance for the PORTA SOLDER 1090 W, a Alloy, Gold-based Noble Metal (Class II — Special Controls, product code EJT), submitted by Wieland Dental + Technik GmbH & Co. KG (Pforzheim, DE). The FDA issued a Cleared decision on May 20, 2004, 80 days after receiving the submission on March 1, 2004. This device falls under the Dental review panel. Regulated under 21 CFR 872.3060.
| 510(k) Number | K040524 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 01, 2004 |
| Decision Date | May 20, 2004 |
| Days to Decision | 80 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EJT — Alloy, Gold-based Noble Metal |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3060 |