| Primary Device ID | 00810129551785 |
| NIH Device Record Key | 549535f8-6d6f-48fd-91c0-ec37582d795f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OvertureTi |
| Version Model Number | PKG-90-OSP-360017 |
| Company DUNS | 119105665 |
| Company Name | Overture Orthopaedics |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| 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 |