Apatech , Ltd. · Class II · Cleared Sep 11, 2008
| K-number | K082073 |
| Device name | ACTIFUSE FLOW BONE GRAFT SUBSTITUTE |
| Applicant | Apatech , Ltd. |
| Product code | MQV |
| Device class | Class II |
| Decision date | Sep 11, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 888.3045 |
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