Vilex, Inc. · Class II · Cleared Mar 18, 2002
| K-number | K014154 |
| Device name | VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00 |
| Applicant | Vilex, Inc. |
| Product code | HWC |
| Device class | Class II |
| Decision date | Mar 18, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 888.3040 |
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