| Primary Device ID | 00889095998696 |
| NIH Device Record Key | 103cae8d-5b29-44ed-8262-893703dfc849 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CROSSWAY |
| Version Model Number | 6177.2111 |
| Company DUNS | 139105691 |
| Company Name | GLOBUS MEDICAL, 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(610)930-1800 |
| info@globusmedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889095998696 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889095998696]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-07-22 |
| Device Publish Date | 2019-07-12 |
| 00889095998696 | Adjustable Depth Stop, 18-26mm |
| 00889095998689 | Harvesting Mill, 6mm |
| 00889095998634 | Temporary Fixation Screw, 10mm |
| 00889095741025 | Adjustable Depth Stop, 10-18mm |
| 00889095740998 | Channel Guide, Right 10° |
| 00889095740981 | Adjustable Channel Guide |
| 00889095740974 | Channel Guide, Left 10° |
| 00889095740929 | Fixation Screw Driver |
| 00889095998672 | Pilot Drill, 2mm |
| 00889095998658 | Temporary Fixation Screw, 14mm |
| 00889095998641 | Temporary Fixation Screw, 12mm |
| 00889095998665 | Temporary Fixation Screw, 16mm |