Idys®-ALIF ZP 3DTI 45573610-S
GUDID 03700780631643
ALIF CAGE
CLARIANCE
Metallic spinal interbody fusion cage| Primary Device ID | 03700780631643 |
| NIH Device Record Key | b151df99-349b-47cb-9b60-a6fb3ac10ad7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Idys®-ALIF ZP 3DTI |
| Version Model Number | 45573610-S |
| Catalog Number | 45573610-S |
| Company DUNS | 296568400 |
| Company Name | CLARIANCE |
| 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 | true |
| 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 | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us | |
| Phone | +1 773 868 7041 |
| s.chambat@clariance-spine.us |
Device Dimensions
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
| Angle | 10 degree |
| Width | 40 Millimeter |
| Height | 16 Millimeter |
| Depth | 30 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700780631643 [Primary] |
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-07 |
| Device Publish Date | 2020-06-29 |
On-Brand Devices [Idys®-ALIF ZP 3DTI]
Trademark Results [Idys]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 IDYS 79237665 5682795 Live/Registered |
CLARIANCE 2018-04-11 |
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