| Primary Device ID | 00810129551815 |
| NIH Device Record Key | 18f310ef-67b0-4c53-8a13-996abb1e53bf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OvertureTi |
| Version Model Number | PKG-90-OSP-400000 |
| 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 |