Primary Device ID | 10888857556072 |
NIH Device Record Key | 4414e23c-d5bd-4d30-b744-1b0a75f7a8fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CASCADIA Interbody System |
Version Model Number | 8030-90032 |
Catalog Number | 8030-90032 |
Company DUNS | 146060863 |
Company Name | K2M, 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 |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com | |
Phone | +1(571)919-2000 |
mark.zellers@stryker.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10888857556072 [Primary] |
OVD | Intervertebral fusion device with integrated fixation, lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
[10888857556072]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-12 |
Device Publish Date | 2024-01-04 |
10888857551817 | Inserter Inner Shaft |
10888857551800 | Inserter Outer Shaft |
10888857462168 | ALIF Trial Inserter |
10888857431461 | Tapered Driver Size 20 |
10888857383838 | Inserter Blade Tether |
10888857383821 | Plate Assembly Final Tightener |
10888857383715 | Plate Assembly Driver Tapered |
10888857320673 | Graft Contaiment Ramp Size 22 mm, Stop |
10888857272170 | Implant Inserter |
10888857562943 | Caddy |
10888857562936 | Caddy |
10888857562929 | Caddy |
10888857562912 | Caddy |
10888857557277 | Inserter ATP, 35° |
10888857557260 | Inserter ATP, 25° |
10888857556072 | Inserter Inner Shaft ATP |
10888857554269 | Untightening Ring Inserter |
07613327506808 | Case Lid |
07613327506761 | Instrument Case |
07613327506624 | Instrument Case |
07613327506570 | Instrument Case |