Altatec GmbH · Class II · Cleared Jan 30, 2009
| K-number | K083496 |
| Device name | CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS |
| Applicant | Altatec GmbH |
| Product code | DZE |
| Device class | Class II |
| Decision date | Jan 30, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 872.3640 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov