| Primary Device ID | 00643169674806 | 
| NIH Device Record Key | b71dc36c-41cd-414c-ada8-3c0c7a706e9c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Capstone Control Spinal System | 
| Version Model Number | 4031527 | 
| Company DUNS | 830350380 | 
| Company Name | MEDTRONIC SOFAMOR DANEK, INC. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| 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 | true | 
| RX Perscription | false | 
| OTC Over-The-Counter | false | 
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Length | 27 Millimeter | 
| Angle | 24 degree | 
| Height | 15 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00643169674806 [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 | 2023-10-10 | 
| Device Publish Date | 2023-10-02 | 
| 00643169677920 | SPACER 4031822 CONTROL 24 DEG 18X22 | 
| 00643169677913 | SPACER 4031722 CONTROL 24 DEG 17X22 | 
| 00643169677906 | SPACER 4031622 CONTROL 24 DEG 16X22 | 
| 00643169677890 | SPACER 4031522 CONTROL 24 DEG 15X22 | 
| 00643169677883 | SPACER 4031422 CONTROL 24 DEG 14X22 | 
| 00643169677876 | SPACER 4031322 CONTROL 24 DEG 13X22 | 
| 00643169674806 | SPACER 4031527 CONTROL 24 DEG 15X27 |