| K-number | K030871 |
| Device name | FIDJI LARGE CEMENT RESTRICTOR |
| Applicant | Spine Next SA |
| Product code | JDK |
| Device class | Class II |
| Decision date | Dec 22, 2003 |
| Decision | Unknown |
| Regulation | 878.3300 |
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