XLIF
GUDID 00887517097002
Tray Base, XLIF Long Instruments
Nuvasive, Inc.
Device sterilization/disinfection container, reusable| Primary Device ID | 00887517097002 |
| NIH Device Record Key | 4996ddec-bc29-48f7-9360-5018db51e2d0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | XLIF |
| Version Model Number | 1545181 |
| 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 | 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 |
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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517097002 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K143579
FDA Product Code
| KCT | Sterilization wrap containers, trays, cassettes & other accessories |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
[00887517097002]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-14 |
| Device Publish Date | 2023-09-06 |
On-Brand Devices [XLIF]
| 00887517526540 | XLIF Thoracic Ins Set |
| 00887517526465 | XLIF Revision Ins Set |
| 00887517526335 | XLIF Long Ins Set |
| 00887517526328 | XLIF Instruments 2 |
| 00887517526311 | XLIF Instruments 1 |
| 00887517526281 | XLIF Corpectomy Ins Set |
| 00887517526267 | XLIF Angled Ins Set |
| 00887517526243 | XLIF II Ins Set |
| 00887517517357 | 40MM Guided Broach Set |
| 00887517517258 | BETA MaXcess Pin Traction Set |
| 00887517516039 | ALPHA XLIF Slide Set |
| 00887517515995 | Alpha XLIF Instruments 2 |
| 00887517515988 | Alpha XLIF Instruments 1 |
| 00887517504180 | XLIF Corpectomy Osteotome, 25mm |
| 00887517504173 | XLIF Corpectomy Osteotome, 15mm |
| 00887517504081 | XLIF Corp Blade, 90mm Lung Retractor Nrw |
| 00887517504074 | XLIF Corp Blade, 80mm Lung Retractor Nrw |
| 00887517464972 | XLIF Rasp, 14mm Offset |
| 00887517464965 | XLIF Curette, Ring Offset Up Down |
| 00887517464958 | XLIF Cutter, 8x14mm Annulus Offset |
| 00887517464941 | XLIF Cutter, 6x14mm Annulus Offset |
| 00887517464934 | XLIF Cobb, Offset Right |
| 00887517464927 | XLIF Cobb, Offset Left |
| 00887517464910 | XLIF Curette, 45° Down Large |
| 00887517464903 | XLIF Curette, 45° Up Large |
| 00887517464590 | XLIF Curette, 90° Down Large |
| 00887517464583 | XLIF Curette, 90° Up Large |
| 00887517464576 | XLIF Curette, 45° Down Small |
| 00887517464569 | XLIF Curette, 45° Up Small |
| 00887517464552 | XLIF Curette, 90° Down Small |
| 00887517464545 | XLIF Curette, 90° Up Small |
| 00887517461377 | ALGI Cobb, Down Large Short |
| 00887517461360 | ALGI Cobb, Down Small Short |
| 00887517461353 | ALGI Cobb, 8° Angled Down Small |
| 00887517461346 | ALGI Cobb, 8° Angled Up Small |
| 00887517461339 | ALGI Cobb, 8° Angled Down Large |
| 00887517461322 | ALGI Cobb, 8° Angled Up Large |
| 00887517453105 | XLIF Pituitary, Angled Left Medium |
| 00887517452795 | XLIF Pituitary, Angled Right Medium |
| 00887517452788 | XLIF Pituitary, Large |
| 00887517452771 | XLIF Pituitary, Medium |
| 00887517452764 | XLIF Pituitary, Small |
| 00887517452757 | XLIF Kerrison, 5mm |
| 00887517452740 | XLIF Kerrison, 2mm |
| 00887517418616 | CoRoent XLT Inserter Trial, Long |
| 00887517417282 | XLIF Annulus Cutter, 6x22mm Angled |
| 00887517417275 | XLIF Annulus Cutter, 6x18mm Angled |
| 00887517417268 | XLIF Annulus Cutter, 6x16mm Angled |
| 00887517417251 | XLIF Annulus Cutter, 6x14mm Angled |
| 00887517417244 | XLIF Annulus Cutter, 4x22mm Angled |
Trademark Results [XLIF]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 XLIF 76203717 2992761 Live/Registered |
NUVASIVE, INC. 2001-01-31 |
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