Smith & Nephew, Inc. · Class II · Cleared Dec 20, 2007
| K-number | K073175 |
| Device name | JOURNEY UNICONDYLAR FEMORAL IMPLANT |
| Applicant | Smith & Nephew, Inc. |
| Product code | HSX |
| Device class | Class II |
| Decision date | Dec 20, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 888.3520 |
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