| Primary Device ID | 00880304691018 |
| NIH Device Record Key | 42a20d51-6bea-443f-a5e0-41a1b6f8dbe6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ARCOS ONE-PIECE REVISION SYSTEM |
| Version Model Number | 11-304024 |
| Catalog Number | 11-304024 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 |