| Primary Device ID | M711AB2040120 |
| NIH Device Record Key | 90129488-20a9-42c0-bb84-eef4b7f3ad21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A-Box® |
| Version Model Number | AB204012 |
| Catalog Number | AB204012 |
| Company DUNS | 156567492 |
| Company Name | Innovasis, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 |
| Phone | 801-261-2236 |
| info@innovasis.com |
| Angle | 12 degree |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M711AB2040120 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M711AB2040120]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-01-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() A-BOX 78877528 3707059 Live/Registered |
Innovasis 2006-05-05 |