| Primary Device ID | 04712602348973 |
| NIH Device Record Key | 5b623b07-7f5f-41c3-b813-eb949ba6167f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Femoral augment, Posterior |
| Version Model Number | 2603-5021 |
| Catalog Number | 2603-5021 |
| Company DUNS | 656700556 |
| Company Name | UNITED ORTHOPEDIC CORP. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| 04712771480177 | Femoral augment, Posterior, #6, 8mm |
| 04712771480160 | Femoral augment, Posterior, #6, 4mm |
| 04712602349048 | Femoral augment, Posterior, #5, 8mm |
| 04712602349031 | Femoral augment, Posterior, #5, 4mm |
| 04712602349024 | Femoral augment, Posterior, #4, 8mm |
| 04712602349017 | Femoral augment, Posterior, #4, 4mm |
| 04712602349000 | Femoral augment, Posterior, #3, 8mm |
| 04712602348997 | Femoral augment, Posterior, #3, 4mm |
| 04712602348980 | Femoral augment, Posterior, #2, 8mm |
| 04712602348973 | Femoral augment, Posterior, #2, 4mm |
| 04712602348966 | Femoral augment, Posterior, #1, 8mm |
| 04712602348959 | Femoral augment, Posterior, #1, 4mm |