| Primary Device ID | 00889024320734 |
| NIH Device Record Key | 135aacd2-fc1e-4e64-974c-61876ab79e8d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BP® |
| Version Model Number | 07.00008.046 |
| 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 |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 21 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024320734 [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 | 2015-10-22 |
| 00889024320741 | 07.00008.047 |
| 00889024320734 | 07.00008.046 |
| 00889024320727 | 07.00008.039 |
| 00889024320710 | 07.00008.038 |
| 00889024320703 | 07.00008.031 |
| 00889024320697 | 07.00008.030 |
| 00889024320680 | 07.00008.023 |
| 00889024320673 | 07.00008.022 |
| 00889024320666 | 07.00008.015 |
| 00889024320659 | 07.00008.014 |
| 00889024320642 | 07.00008.007 |
| 00889024338579 | 8002-1724-00 |
| 00889024338562 | 8002-1720-00 |
| 00889024338555 | 8002-1524-00 |
| 00889024338548 | 8002-1520-00 |