| Primary Device ID | 04712771480061 |
| NIH Device Record Key | 490ca6ba-1e71-4e61-bf8a-9386588d261c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tibial Baseplate, PSA type, Screw locking |
| Version Model Number | 2203-5230 |
| Catalog Number | 2203-5230 |
| 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 |
| 04712771480092 | Tibial Baseplate, PSA type, Screw locking, #6 |
| 04712771480085 | Tibial Baseplate, PSA type, Screw locking, #5 |
| 04712771480078 | Tibial Baseplate, PSA type, Screw locking, #4 |
| 04712771480061 | Tibial Baseplate, PSA type, Screw locking, #3 |
| 04712771480054 | Tibial Baseplate, PSA type, Screw locking, #2 |
| 04712771480047 | Tibial Baseplate, PSA type, Screw locking, #1 |