| Primary Device ID | 10840642107579 |
| NIH Device Record Key | 40d66f44-2fb6-4423-9d21-b0ae801d01be |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | True Position® Spacer System |
| Version Model Number | 1208-01-3010 |
| Catalog Number | 1208-01-3010 |
| Company DUNS | 067789763 |
| Company Name | Spine Wave, 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 | 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 | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com | |
| Phone | 203-944-9494 |
| GUDID@spinewave.com |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Height | 10 Millimeter |
| Length | 30 Millimeter |
| Angle | 7 degree |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10840642107579 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
[10840642107579]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2016-09-24 |
| 10840642107890 | XL Implant Inserter Assembly |
| 10840642107883 | Implant Inserter |
| 10840642107722 | Implant, 36 (L) x 7.5 (H) mm |
| 10840642107715 | Implant, 30 (L) x 7.5 (H) mm |
| 10840642107708 | Implant, 27 (L) x 7.5 (H) mm |
| 10840642107692 | Implant, Lordotic, 36 (L) x 15 (H) mm, 7° |
| 10840642107685 | Implant, Lordotic, 36 (L) x 14 (H) mm, 7° |
| 10840642107678 | Implant, Lordotic, 36 (L) x 13 (H) mm, 7° |
| 10840642107661 | Implant, Lordotic, 36 (L) x 12 (H) mm, 7° |
| 10840642107654 | Implant, Lordotic, 36 (L) x 11 (H) mm, 7° |
| 10840642107647 | Implant, Lordotic, 36 (L) x 10 (H) mm, 7° |
| 10840642107630 | Implant, Lordotic, 36 (L) x 9 (H) mm, 7° |
| 10840642107623 | Implant, Lordotic, 30 (L) x 15 (H) mm, 7° |
| 10840642107616 | Implant, Lordotic, 30 (L) x 14 (H) mm, 7° |
| 10840642107609 | Implant, Lordotic, 30 (L) x 13 (H) mm, 7° |
| 10840642107593 | Implant, Lordotic, 30 (L) x 12 (H) mm, 7° |
| 10840642107586 | Implant, Lordotic, 30 (L) x 11 (H) mm, 7° |
| 10840642107579 | Implant, Lordotic, 30 (L) x 10 (H) mm, 7° |
| 10840642107562 | Implant, Lordotic, 30 (L) x 9 (H) mm, 7° |
| 10840642107555 | Implant, Lordotic, 27 (L) x 15 (H) mm, 7° |
| 10840642107548 | Implant, Lordotic, 27 (L) x 14 (H) mm, 7° |
| 10840642107531 | Implant, Lordotic, 27 (L) x 13 (H) mm, 7° |
| 10840642107524 | Implant, Lordotic, 27 (L) x 12 (H) mm, 7° |
| 10840642107517 | Implant, Lordotic, 27 (L) x 11 (H) mm, 7° |
| 10840642107500 | Implant, Lordotic, 27 (L) x 10 (H) mm, 7° |
| 10840642107494 | Implant, Lordotic, 27 (L) x 9 (H) mm, 7° |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TRUE POSITION 86258168 4652227 Live/Registered |
Dayton Progress Corporation 2014-04-21 |
![]() TRUE POSITION 77909781 3948826 Live/Registered |
SPINE WAVE, INC. 2010-01-12 |
![]() TRUE POSITION 75336437 not registered Dead/Abandoned |
EXSYS Tool, Inc. 1997-08-05 |
![]() TRUE POSITION 74638035 1946974 Live/Registered |
Modern Builders Supply, Inc. 1995-02-22 |
![]() TRUE POSITION 74604318 not registered Dead/Abandoned |
Associated RT, Inc. 1994-11-29 |
![]() TRUE POSITION 73435836 1326563 Live/Registered |
Dayton Progress Corporation 1983-07-22 |