| Primary Device ID | 00810136252330 |
| NIH Device Record Key | db1fbb2d-1499-470a-a645-accc95c1342e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ZSFab Lumbar Interbody System |
| Version Model Number | 28101408 |
| Company DUNS | 105224126 |
| Company Name | Zsfab, 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 | 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 |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Depth | 28 Millimeter |
| Width | 10 Millimeter |
| Height | 14 Millimeter |
| Angle | 8 degree |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810136252330 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-19 |
| Device Publish Date | 2025-05-11 |
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| 00810136252422 | Lumbar-TLIF 31Dx12Wx09Hx8° |
| 00810136252415 | Lumbar-TLIF 31Dx12Wx08Hx8° |
| 00810136252408 | Lumbar-TLIF 31Dx12Wx14Hx4° |