Submission Details
| 510(k) Number | K033629 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 19, 2003 |
| Decision Date | December 22, 2003 |
| Days to Decision | 33 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
K033629 is an FDA 510(k) clearance for the VERSYO.BOND, a Resin, Denture, Relining, Repairing, Rebasing (Class II — Special Controls, product code EBI), submitted by Heraeus Kulzer, Inc. (South Bend, US). The FDA issued a Cleared decision on December 22, 2003, 33 days after receiving the submission on November 19, 2003. This device falls under the Dental review panel. Regulated under 21 CFR 872.3760.
| 510(k) Number | K033629 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 19, 2003 |
| Decision Date | December 22, 2003 |
| Days to Decision | 33 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | EBI — Resin, Denture, Relining, Repairing, Rebasing |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3760 |