| Primary Device ID | 00889024333352 |
| NIH Device Record Key | 132c89e8-df8a-4d20-a655-9248df733700 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BAK® |
| Version Model Number | 3000-1924-00 |
| Company DUNS | 787663400 |
| Company Name | ZIMMER SPINE, 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 |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Outer Diameter | 19 Millimeter |
| Length | 24 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024333352 [Primary] |
| MAX | Intervertebral fusion device with bone graft, lumbar |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-09-24 |
| 00889024333352 | 3000-1924-00 |
| 00889024333345 | 3000-1920-00 |
| 00889024333338 | 3000-1732-00 |
| 00889024333321 | 3000-1728-00 |
| 00889024333314 | 3000-1724-00 |
| 00889024333307 | 3000-1720-00 |
| 00889024333291 | 3000-1532-00 |
| 00889024333284 | 3000-1528-00 |
| 00889024333277 | 3000-1524-00 |
| 00889024333260 | 3000-1520-00 |
| 00889024333253 | 3000-1344-00 |
| 00889024333246 | 3000-1340-00 |
| 00889024333239 | 3000-1336-00 |
| 00889024333222 | 3000-1332-00 |
| 00889024333215 | 3000-1328-00 |
| 00889024333208 | 3000-1324-00 |
| 00889024333192 | 3000-1320-00 |
| 00889024333185 | 3000-1140-00 |
| 00889024333178 | 3000-1136-00 |
| 00889024333161 | 3000-1132-00 |
| 00889024333154 | 3000-1128-00 |
| 00889024333147 | 3000-1126-00 |
| 00889024333130 | 3000-1124-00 |
| 00889024333123 | 3000-1120-00 |
| 00889024333116 | 3000-0932-00 |
| 00889024333109 | 3000-0926-00 |
| 00889024333093 | 3000-0924-00 |
| 00889024333086 | 3000-0920-00 |