| Primary Device ID | 00887517389794 |
| NIH Device Record Key | 130dd610-1052-48b1-b676-bf367bbe4387 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Graft Integration |
| Version Model Number | 6910122 |
| 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 | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517389794 [Primary] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887517389794]
Moist Heat or Steam Sterilization
[00887517389794]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-25 |
| Device Publish Date | 2018-09-24 |
| 00887517525079 | TL Graft Containment Set |
| 00887517515872 | ALPHA TL Graft Integration Set |
| 00887517389794 | Graft Integration Plug Pusher, Allograft |
| 00887517389787 | Graft Integration Plug Cutter, Allograft |
| 00887517243560 | Graft Integration Pusher, Graft |
| 00887517243546 | Graft Integration Pusher, Trough |
| 00887517834515 | XLIF Handle, Graft Containment Slide |
| 00887517244048 | Graft Containment Base, TL Tray |
| 00887517243195 | TL - Graft Containment Set (Base) |
| 00887517243508 | Graft Integration Loading Block, Implant |