| K-number | K231503 |
| Device name | CUPTIMIZE Advanced |
| Applicant | DePuy Orthopaedics, Inc. |
| Product code | LLZ |
| Device class | Class II |
| Decision date | Aug 22, 2023 |
| Decision | Substantially Equivalent |
| Regulation | 892.2050 |
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