Orthovita, Inc. · Class II · Cleared Aug 29, 2003
| K-number | K032409 |
| Device name | VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER |
| Applicant | Orthovita, Inc. |
| Product code | MQV |
| Device class | Class II |
| Decision date | Aug 29, 2003 |
| 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