| K-number | K792181 |
| Device name | 3M HS 22 FEMORAL COMPONENT |
| Applicant | 3M Company |
| Product code | KWL |
| Device class | Class II |
| Decision date | Nov 15, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 888.3360 |
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