| Primary Device ID | 00887517707482 |
| NIH Device Record Key | 1ec48350-92e7-4dc3-a86a-0f98842ad9c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Graft Delivery System |
| Version Model Number | 5120931 |
| Company DUNS | 053950783 |
| Company Name | Nuvasive, Inc. |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517707482 [Primary] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887517707482]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-21 |
| Device Publish Date | 2018-09-24 |
| 00887517518873 | Graft Delivery System |
| 00887517452719 | GDS Graft Pusher |
| 00887517397898 | GDS Graft Pusher |
| 00887517397881 | GDS K-Wire, Funnel Cap |
| 00887517397867 | GDS Graft Funnel |
| 00887517397829 | GDS Graft Tube |
| 00887517213136 | GDS Counter-Torque |
| 00887517213129 | GDS Graft Pusher |
| 00887517212696 | GDS Graft Removal Tool |
| 00887517707505 | GDS Tube, Tapered Small |
| 00887517707482 | GDS Tube, 8.4mm Curved |
| 00887517707475 | GDS Tube, 7.5mm Curved |
| 00887517707499 | GDS Applicator, Ø5mm Threaded |