| Primary Device ID | 03701337615604 |
| NIH Device Record Key | b3084553-beac-44bc-9b50-39d352c3d3d4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Triway |
| Version Model Number | N20 ST725 |
| Catalog Number | N20 ST725 |
| Company DUNS | 263616749 |
| Company Name | IN2BONES |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03701337615604 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-23 |
| Device Publish Date | 2024-12-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TRIWAY 79154341 4702022 Live/Registered |
In2Bones 2014-06-04 |