| Primary Device ID | 00840420115249 |
| NIH Device Record Key | f700e6d8-8da1-4ad3-b7d7-31e145fda23b |
| Commercial Distribution Discontinuation | 2016-03-07 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ORTHOLOC 3Di |
| Version Model Number | 59224516 |
| Company DUNS | 807201207 |
| Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
| 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 | true |
| 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 |