Institut Straumann AG · Class II · Cleared Feb 13, 1990
| K-number | K894594 |
| Device name | BONEFIT HOLLOW SCREW IMPLANTS |
| Applicant | Institut Straumann AG |
| Product code | DZE |
| Device class | Class II |
| Decision date | Feb 13, 1990 |
| 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