Idys®-ALIF TiVac 42523418-S
GUDID 03700780629442
ALIF CAGE
CLARIANCE
Polymeric spinal fusion cage, sterile| Primary Device ID | 03700780629442 |
| NIH Device Record Key | 3e6cd2ed-2c65-42d7-9abf-9b2dfa24cffb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Idys®-ALIF TiVac |
| Version Model Number | 42523418-S |
| Catalog Number | 42523418-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 | true |
| 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 |
Device Dimensions
| Width | 40 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700780629442 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K191263
FDA Product Code
| OVD | Intervertebral fusion device with integrated fixation, 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 | 2019-12-23 |
| Device Publish Date | 2019-12-14 |
On-Brand Devices [Idys®-ALIF TiVac]
Trademark Results [Idys]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 IDYS 79237665 5682795 Live/Registered |
CLARIANCE 2018-04-11 |
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