ALIF
GUDID 00887517621771
ALIF Interfixated Screw, 5.0x27.5mm Var
Nuvasive, Inc.
Spinal bone screw, non-bioabsorbable| Primary Device ID | 00887517621771 |
| NIH Device Record Key | 66292632-ef63-479a-8406-6eca7a006977 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ALIF |
| Version Model Number | 1770834 |
| Company DUNS | 053950783 |
| Company Name | Nuvasive, 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 | true |
| 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 |
Customer Support Contacts
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com | |
| Phone | +1800-475-9131 |
| nuvainfo@globusmedical.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517621771 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K151214
FDA Product Code
| OVD | Intervertebral fusion device with integrated fixation, lumbar |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
[00887517621771]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-04-09 |
| Device Publish Date | 2016-01-18 |
On-Brand Devices [ALIF]
| 00887517514806 | Alpha ALIF Instruments 3 |
| 00887517514790 | Alpha ALIF Instruments 2 |
| 00887517514783 | Alpha ALIF Instruments 1 |
| 00887517256065 | ALIF Distractor, Lordotic Large |
| 00887517256058 | ALIF Distractor, Lordotic Small |
| 00887517149145 | ALIF Cobb, 26mm Lg Straight |
| 00887517149138 | ALIF Cobb, 22mm Med Straight |
| 00887517149121 | ALIF Cobb, 26mm Lg Down Angled |
| 00887517149114 | ALIF Cobb, 22mm Med Down Angled |
| 00887517149107 | ALIF Curette, 12x8 Lg Down Angled |
| 00887517148698 | ALIF Curette, 10x6 Med Down Angled |
| 00887517148681 | ALIF Curette, 8x4 Sm Down Angled |
| 00887517148674 | ALIF Curette, 12x8 Lg Up Angled |
| 00887517148667 | ALIF Curette, 10x6 Med Up Angled |
| 00887517148650 | ALIF Curette, 8x4 Sm Up Angled |
| 00887517148643 | ALIF Curette, 12x8 Lg Straight |
| 00887517148636 | ALIF Curette, 10x6 Med Straight |
| 00887517148629 | ALIF Curette, 8x4 Sm Straight |
| 00887517148612 | ALIF Rasp, 38mm Large Straight |
| 00887517148605 | ALIF Rasp, 34mm Small Straight |
| 00887517147646 | ALIF Chisel, Medium Angled |
| 00887517147639 | ALIF Chisel, Medium Straight |
| 00887517147622 | ALIF Chisel, Small Angled |
| 00887517147615 | ALIF Chisel, Small Straight |
| 00887517622099 | ALIF Interfixated Screw, 6.0x27.5mm Fix |
| 00887517622082 | ALIF Interfixated Screw, 6.0x25.0mm Fix |
| 00887517622075 | ALIF Interfixated Screw, 6.0x22.5mm Fix |
| 00887517622068 | ALIF Interfixated Screw, 6.0x20.0mm Fix |
| 00887517622051 | ALIF Interfixated Screw, 5.0x27.5mm Fix |
| 00887517622044 | ALIF Interfixated Screw, 5.0x25.0mm Fix |
| 00887517622037 | ALIF Interfixated Screw, 5.0x22.5mm Fix |
| 00887517622020 | ALIF Interfixated Screw, 5.0x20.0mm Fix |
| 00887517622013 | ALIF Interfixated Screw, 6.0x27.5mm Var |
| 00887517622006 | ALIF Interfixated Screw, 6.0x25.0mm Var |
| 00887517621795 | ALIF Interfixated Screw, 6.0x22.5mm Var |
| 00887517621788 | ALIF Interfixated Screw, 6.0x20.0mm Var |
| 00887517621771 | ALIF Interfixated Screw, 5.0x27.5mm Var |
| 00887517621764 | ALIF Interfixated Screw, 5.0x25.0mm Var |
| 00887517621757 | ALIF Interfixated Screw, 5.0x22.5mm Var |
| 00887517621740 | ALIF Interfixated Screw, 5.0x20.0mm Var |
| 00887517672728 | ALIF Interfixated Inserter, Interbody |
| 00887517626776 | ALIF Interfixated Inserter, Antero 38 UP |
| 00887517626769 | ALIF Interfixated Inserter, Antero 38 DN |
| 00887517626752 | ALIF Interfixated Inserter, Antero 34 UP |
| 00887517626745 | ALIF Interfixated Inserter, Antero 34 DN |
| 00887517626738 | ALIF Interfixated Inserter, Interbody |
| 00887517149152 | ALIF Endplate Scraper, Push-Pull |
| 00887517987938 | ALIF Retractor 50mm Wide Blades |
| 00887517973054 | ALIF Blade, 220mm Wide |
| 00887517973047 | ALIF Blade, 200mm Wide |
Trademark Results [ALIF]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ALIF 98321291 not registered Live/Pending |
Sanreta, Rose 2023-12-19 |
 ALIF 90830635 not registered Live/Pending |
Muhammad Mirza 2021-07-15 |
 ALIF 90695436 not registered Live/Pending |
Dongguan Airifu Technology Co., Ltd. 2021-05-07 |
 ALIF 90688164 not registered Live/Pending |
Alif Semiconductor, Inc. 2021-05-03 |
 ALIF 88868763 not registered Live/Pending |
Minder Apps, Inc. 2020-04-12 |
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