| Primary Device ID | 00880304283220 |
| NIH Device Record Key | fe9c1a2d-9b7e-4d63-9c4b-01ae6c229c3f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REPICCI II RESURFACING KNEE SYSTEM |
| Version Model Number | 215081 |
| Catalog Number | 215081 |
| 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 |