Protek, Inc. · Class II · Cleared Jul 19, 1989
| K-number | K892059 |
| Device name | FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR |
| Applicant | Protek, Inc. |
| Product code | LZY |
| Device class | Class II |
| Decision date | Jul 19, 1989 |
| 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