Other products from "ZIMMER SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024331891 1875-314 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
2 00889024331884 1875-312 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
3 00889024331877 1875-310 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
4 00889024331860 1875-308 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
5 00889024331853 1875-114 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
6 00889024331846 1875-112 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
7 00889024331839 1875-110 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
8 00889024331822 1875-108 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
9 00889024331815 1874-500 1874-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
10 00889024331808 1874-300 1874-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
11 00889024331792 1874-100 1874-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
12 00889024331785 1873-1 1873-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
13 00889024331778 1872-2 1872-2 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
14 00889024332041 1894-400 1894-400 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
15 00889024331761 1871-1 1871-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
16 00889024331747 1869-1 1869-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
17 00889024331730 1868-14 1868-14 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
18 00889024331723 1868-12 1868-12 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
19 00889024331716 1868-10 1868-10 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
20 00889024331709 1868-08 1868-08 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
21 00889024331693 1865-514 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
22 00889024331686 1865-512 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
23 00889024332058 1894-500 1894-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
24 00889024332034 1894-300 1894-300 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
25 00889024332027 1894-200 1894-200 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
26 00889024332010 1894-100 1894-100 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
27 00889024332003 1879-500 1879-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
28 00889024331990 1879-300 1879-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
29 00889024331983 1879-100 1879-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
30 00889024331976 1877-500 1877-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
31 00889024331969 1877-300 1877-300 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
32 00889024331952 1877-100 1877-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
33 00889024331945 1876-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
34 00889024331938 1875-514 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
35 00889024331921 1875-512 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
36 00889024331914 1875-510 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
37 00889024331907 1875-508 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
38 00889024331679 1865-510 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
39 00889024331662 1865-508 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
40 00889024331655 1865-314 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
41 00889024331648 1865-312 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
42 00889024331631 1865-310 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
43 00889024331624 1865-308 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
44 00889024331617 1865-114 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
45 00889024331600 1865-112 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
46 00889024331594 1865-110 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
47 00889024331587 1865-108 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
48 00889024331563 1859-1 1859-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
49 00889024331556 1857-500 1857-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
50 00889024331549 1857-300 1857-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
Other products with the same Product Codes "MQP, MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 07640450869326 SPE-US 3L 26-N SPE-US 3L 26-N SMOOTH HL TRIAL LARGE H26 LORDOSIS 30° SCARLET® AL-T SPINEART SA
2 07640450869319 SPE-US 3L 24-N SPE-US 3L 24-N SMOOTH HL TRIAL LARGE H24 LORDOSIS 30° SCARLET® AL-T SPINEART SA
3 07640450869302 SPE-US 3L 22-N SPE-US 3L 22-N SMOOTH HL TRIAL LARGE H22 LORDOSIS 30° SCARLET® AL-T SPINEART SA
4 07640450869296 SPE-US 3L 20-N SPE-US 3L 20-N SMOOTH HL TRIAL LARGE H20 LORDOSIS 30° SCARLET® AL-T SPINEART SA
5 07640450869289 SPE-US 2L 25-N SPE-US 2L 25-N SMOOTH HL TRIAL LARGE H25 LORDOSIS 25° SCARLET® AL-T SPINEART SA
6 07640450869272 SPE-US 2L 23-N SPE-US 2L 23-N SMOOTH HL TRIAL LARGE H23 LORDOSIS 25° SCARLET® AL-T SPINEART SA
7 07640450869265 SPE-US 2L 21-N SPE-US 2L 21-N SMOOTH HL TRIAL LARGE H21 LORDOSIS 25° SCARLET® AL-T SPINEART SA
8 07640450869258 SPE-US 2L 19-N SPE-US 2L 19-N SMOOTH HL TRIAL LARGE H19 LORDOSIS 25° SCARLET® AL-T SPINEART SA
9 07640450869241 SPE-US 1L 21-N SPE-US 1L 21-N SMOOTH HL TRIAL LARGE H21 LORDOSIS 20° SCARLET® AL-T SPINEART SA
10 07640450869234 SPE-US 1L 19-N SPE-US 1L 19-N SMOOTH HL TRIAL LARGE H19 LORDOSIS 20° SCARLET® AL-T SPINEART SA
11 07640450869227 SPE-US 1L 17-N SPE-US 1L 17-N SMOOTH HL TRIAL LARGE H17 LORDOSIS 20° SCARLET® AL-T SPINEART SA
12 07640450869210 SPE-US 1L 15-N SPE-US 1L 15-N SMOOTH HL TRIAL LARGE H15 LORDOSIS 20° SCARLET® AL-T SPINEART SA
13 07640450869203 SPE-US 3M 25-N SPE-US 3M 25-N SMOOTH HL TRIAL MEDIUM H25 LORDOSIS 30° SCARLET® AL-T SPINEART SA
14 07640450869197 SPE-US 3M 23-N SPE-US 3M 23-N SMOOTH HL TRIAL MEDIUM H23 LORDOSIS 30° SCARLET® AL-T SPINEART SA
15 07640450869180 SPE-US 3M 21-N SPE-US 3M 21-N SMOOTH HL TRIAL MEDIUM H21 LORDOSIS 30° SCARLET® AL-T SPINEART SA
16 07640450869173 SPE-US 3M 19-N SPE-US 3M 19-N SMOOTH HL TRIAL MEDIUM H19 LORDOSIS 30° SCARLET® AL-T SPINEART SA
17 07640450869166 SPE-US 2M 24-N SPE-US 2M 24-N SMOOTH HL TRIAL MEDIUM H24 LORDOSIS 25° SCARLET® AL-T SPINEART SA
18 07640450869159 SPE-US 2M 22-N SPE-US 2M 22-N SMOOTH HL TRIAL MEDIUM H22 LORDOSIS 25° SCARLET® AL-T SPINEART SA
19 07640450869142 SPE-US 2M 20-N SPE-US 2M 20-N SMOOTH HL TRIAL MEDIUM H20 LORDOSIS 25° SCARLET® AL-T SPINEART SA
20 07640450869135 SPE-US 2M 18-N SPE-US 2M 18-N SMOOTH HL TRIAL MEDIUM H18 LORDOSIS 25° SCARLET® AL-T SPINEART SA
21 07640450869128 SPE-US 1M 20-N SPE-US 1M 20-N SMOOTH HL TRIAL MEDIUM H20 LORDOSIS 20° SCARLET® AL-T SPINEART SA
22 07640450869111 SPE-US 1M 18-N SPE-US 1M 18-N SMOOTH HL TRIAL MEDIUM H18 LORDOSIS 20° SCARLET® AL-T SPINEART SA
23 07640450869104 SPE-US 1M 16-N SPE-US 1M 16-N SMOOTH HL TRIAL MEDIUM H16 LORDOSIS 20° SCARLET® AL-T SPINEART SA
24 07640450869098 SPE-US 1M 14-N SPE-US 1M 14-N SMOOTH HL TRIAL MEDIUM H14 LORDOSIS 20° SCARLET® AL-T SPINEART SA
25 07640450869081 SPE-US 3S 23-N SPE-US 3S 21-N SMOOTH HL TRIAL SMALL H23 LORDOSIS 30° SCARLET® AL-T SPINEART SA
26 07640450869074 SPE-US 3S 21-N SPE-US 3S 21-N SMOOTH HL TRIAL SMALL H21 LORDOSIS 30° SCARLET® AL-T SPINEART SA
27 07640450869067 SPE-US 3S 19-N SPE-US 3S 19-N SMOOTH HL TRIAL SMALL H19 LORDOSIS 30° SCARLET® AL-T SPINEART SA
28 07640450869050 SPE-US 3S 17-N SPE-US 3S 17-N SMOOTH HL TRIAL SMALL H17 LORDOSIS 30° SCARLET® AL-T SPINEART SA
29 07640450869043 SPE-US 2S 21-N SPE-US 2S 21-N SMOOTH HL TRIAL SMALL H21 LORDOSIS 25° SCARLET® AL-T SPINEART SA
30 07640450869036 SPE-US 2S 19-N SPE-US 2S 19-N SMOOTH HL TRIAL SMALL H19 LORDOSIS 25° SCARLET® AL-T SPINEART SA
31 07640450869029 SPE-US 2S 17-N SPE-US 2S 17-N SMOOTH HL TRIAL SMALL H17 LORDOSIS 25° SCARLET® AL-T SPINEART SA
32 07640450869012 SPE-US 2S 15-N SPE-US 2S 15-N SMOOTH HL TRIAL SMALL H15 LORDOSIS 25° SCARLET® AL-T SPINEART SA
33 07640450869005 SPE-US 1S 19-N SPE-US 1S 19-N SMOOTH HL TRIAL SMALL H19 LORDOSIS 20° SCARLET® AL-T SPINEART SA
34 07640450868992 SPE-US 1S 17-N SPE-US 1S 17-N SMOOTH HL TRIAL SMALL H17 LORDOSIS 20° SCARLET® AL-T SPINEART SA
35 07640450868985 SPE-US 1S 15-N SPE-US 1S 15-N SMOOTH HL TRIAL SMALL H15 LORDOSIS 20° SCARLET® AL-T SPINEART SA
36 07640450868978 SPE-US 1S 13-N SPE-US 1S 13-N SMOOTH HL TRIAL SMALL H13 LORDOSIS 20° SCARLET® AL-T SPINEART SA
37 07640450866196 SPE-US 00 92-N SPE-US 00 92-N Windowed Cage and Plate Holder JULIET® Ti LL SPINEART SA
38 07640450863317 DYN-IT 01 03-N DYN-IT 01 03-N IMPLANT HOLDER HANDLE (JULIET ® TL) JULIET TL Instruments SPINEART SA
39 07640450863300 DYN-IT 01 02-N DYN-IT 01 02-N IMPLANT HOLDER TUBE (JULIET ® TL) JULIET TL Instruments SPINEART SA
40 07640450863294 DYN-IT 01 01-N DYN-IT 01 01-N IMPLANT HOLDER SHAFT (JULIET ® TL) JULIET TL Instruments SPINEART SA
41 07640450862624 SPE-US S5 18-N SPE-US S5 18-N SMOOTH TRIAL Small SCARLET® AL-T SPINEART SA
42 07640450862617 SPE-US S0 18-N SPE-US S0 18-N SMOOTH TRIAL Small SCARLET® AL-T SPINEART SA
43 07640450862600 SPE-US M5 18-N SPE-US M5 18-N SMOOTH TRIAL Médium SCARLET® AL-T SPINEART SA
44 07640450862594 SPE-US M0 18-N SPE-US L5 18-N SMOOTH TRIAL Médium SCARLET® AL-T SPINEART SA
45 07640450862587 SPE-US L5 18-N SPE-US L5 18-N SMOOTH TRIAL Large SCARLET® AL-T SPINEART SA
46 07640375235169 SPE-US 01 28-N SPE-US 01 28-N IMPLANT HOLDER-L SCARLET® AL-T SPINEART SA
47 07640375235152 SPE-US 01 27-N SPE-US 01 27-N IMPLANT HOLDER-SM SCARLET® AL-T SPINEART SA
48 07640375235145 SPE-US 01 25-N SPE-US 01 25-N OLIF IMPLANT HOLDER-L SCARLET® AL-T SPINEART SA
49 07640375235138 SPE-US 01 24-N SPE-US 01 24-N OLIF IMPLANT HOLDER-SM SCARLET® AL-T SPINEART SA
50 07640375235107 SPE-US 01 18-N SPE-US 01 18-N THREADED U-JOINT SCARLET® AL-T SPINEART SA