Vilex, Inc. · Class II · Cleared Mar 1, 2004
| K-number | K023684 |
| Device name | CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365 |
| Applicant | Vilex, Inc. |
| Product code | KWD |
| Device class | Class II |
| Decision date | Mar 1, 2004 |
| Decision | Substantially Equivalent |
| Regulation | 888.3730 |
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