No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00887517399779 | 6942044 | CoRoent® XLR, 20x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
2 | 00887517399700 | 6941844 | CoRoent® XLR, 18x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
3 | 00887517399335 | 6941644 | CoRoent® XLR, 16x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
4 | 00887517398765 | 6941444 | CoRoent® XLR, 14x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
5 | 00887517398499 | 6941244 | CoRoent® XLR, 12x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
6 | 00887517398420 | 6941044 | CoRoent® XLR, 10x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
7 | 00887517398055 | 6932088 | CoRoent® XLR, 20x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
8 | 00887517397683 | 6931888 | CoRoent® XLR, 18x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
9 | 00887517397256 | 6931688 | CoRoent® XLR, 16x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
10 | 00887517396822 | 6931488 | CoRoent® XLR, 14x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
11 | 00887517396457 | 6931288 | CoRoent® XLR, 12x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
12 | 00887517395641 | 6922088 | CoRoent® XLR, 20x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
13 | 00887517395634 | 6922044 | CoRoent® XLR, 20x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
14 | 00887517395269 | 6921888 | CoRoent® XLR, 18x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
15 | 00887517395252 | 6921844 | CoRoent® XLR, 18x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
16 | 00887517394880 | 6921688 | CoRoent® XLR, 16x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
17 | 00887517394873 | 6921660 | CoRoent® XL Wide, 16x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
18 | 00887517394866 | 6921655 | CoRoent® XL Wide, 16x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
19 | 00887517394859 | 6921650 | CoRoent® XL Wide, 16x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
20 | 00887517394842 | 6921645 | CoRoent® XL Wide, 16x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
21 | 00887517394835 | 6921644 | CoRoent® XLR, 16x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
22 | 00887517394569 | 6921488 | CoRoent® XLR, 14x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
23 | 00887517394552 | 6921460 | CoRoent® XL Wide, 14x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
24 | 00887517394545 | 6921455 | CoRoent® XL Wide, 14x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
25 | 00887517394538 | 6921450 | CoRoent® XL Wide, 14x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
26 | 00887517394521 | 6921445 | CoRoent® XL Wide, 14x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
27 | 00887517394514 | 6921444 | CoRoent® XLR, 14x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
28 | 00887517394149 | 6921288 | CoRoent® XLR, 12x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
29 | 00887517394132 | 6921260 | CoRoent® XL Wide, 12x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
30 | 00887517394125 | 6921255 | CoRoent® XL Wide, 12x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
31 | 00887517394118 | 6921250 | CoRoent® XL Wide, 12x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
32 | 00887517394101 | 6921245 | CoRoent® XL Wide, 12x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
33 | 00887517393791 | 6921244 | CoRoent® XLR, 12x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
34 | 00887517393722 | 6921088 | CoRoent® XLR, 10x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
35 | 00887517393715 | 6921060 | CoRoent® XL Wide, 10x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
36 | 00887517393708 | 6921055 | CoRoent® XL Wide, 10x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
37 | 00887517393395 | 6921050 | CoRoent® XL Wide, 10x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
38 | 00887517393388 | 6921045 | CoRoent® XL Wide, 10x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
39 | 00887517393371 | 6921044 | CoRoent® XLR, 10x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
40 | 00887517393333 | 6920860 | CoRoent® XL Wide, 8x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
41 | 00887517393326 | 6920855 | CoRoent® XL Wide, 8x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
42 | 00887517393319 | 6920850 | CoRoent® XL Wide, 8x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
43 | 00887517393302 | 6920845 | CoRoent® XL Wide, 8x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
44 | 00887517392961 | 6916860 | CoRoent® XL, 16x18x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
45 | 00887517392954 | 6916855 | CoRoent® XL, 16x18x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
46 | 00887517392947 | 6916850 | CoRoent® XL, 16x18x50mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
47 | 00887517392930 | 6916845 | CoRoent® XL, 16x18x45mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
48 | 00887517392923 | 6916840 | CoRoent® XL, 16x18x40mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
49 | 00887517392916 | 6916260 | CoRoent® XL Wide, 16x22x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
50 | 00887517392909 | 6916255 | CoRoent® XL Wide, 16x22x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00191375036005 | 2156-9319 | 2156-9319 | Trial, 7 Deg Lordotic, X-Large, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
2 | 00191375036012 | 2156-9320 | 2156-9320 | Trial, 7 Deg Lordotic, X-Large, 20mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
3 | 00191375035992 | 2156-9318 | 2156-9318 | Trial, 7 Deg Lordotic, X-Large, 18mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
4 | 00191375035985 | 2156-9317 | 2156-9317 | Trial, 7 Deg Lordotic, X-Large, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
5 | 00191375035978 | 2156-9219 | 2156-9219 | Trial, 7 Deg Lordotic, Large, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
6 | 00191375035961 | 2156-9217 | 2156-9217 | Trial, 7 Deg Lordotic, Large, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
7 | 00191375035954 | 2156-9119 | 2156-9119 | Trial, 7 Deg Lordotic, Standard, 19mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
8 | 00191375035947 | 2156-9117 | 2156-9117 | Trial, 7 Deg Lordotic, Standard, 17mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
9 | 00191375030287 | 2156-9316 | 2156-9316 | Trial, 7 Deg Lordotic, X-Large, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
10 | 00191375030270 | 2156-9216 | 2156-9216 | Trial, 7 Deg Lordotic, Large, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
11 | 00191375030263 | 2156-9116 | 2156-9116 | Trial, 7 Deg Lordotic, Standard, 16mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
12 | 00191375018896 | 2107-0320-S | 2107-0320-S | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
13 | 00191375018889 | 2107-0318-S | 2107-0318-S | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
14 | 00191375018872 | 2107-0220-S | 2107-0220-S | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
15 | 00191375018865 | 2107-0218-S | 2107-0218-S | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
16 | 00191375018858 | 2107-0120-S | 2107-0120-S | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
17 | 00191375018841 | 2107-0118-S | 2107-0118-S | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR Sterile Barrier System | TITAN SPINE, LLC |
18 | 00191375012030 | 2107-0320-N | 2107-0320-N | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | TITAN SPINE, LLC |
19 | 00191375012023 | 2107-0318-N | 2107-0318-N | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | TITAN SPINE, LLC |
20 | 00191375012016 | 2107-0220-N | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
21 | 00191375012009 | 2107-0218-N | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
22 | 00191375011996 | 2107-0120-N | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
23 | 00191375011989 | 2107-0118-N | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR nanoLOCK® Surface Technology | MEDTRONIC SOFAMOR DANEK, INC. | |
24 | 00191375011972 | 1130-1010 | 1130-1010 | Caddy, Large | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
25 | 00191375011965 | 1130-1020 | 1130-1020 | Caddy, Medium | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
26 | 00191375011958 | 1130-1030 | 1130-1030 | Caddy, Small | ENDOSKELETON® Sterile Barrier System | TITAN SPINE, LLC |
27 | 00191375000143 | 2200-0001 | 2200-0001 | Implant Caddy | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
28 | 00191375000051 | 2107-0320 | 2107-0320 | Interbody Fusion Device 7 Degree X-Large 20mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
29 | 00191375000044 | 2107-0318 | 2107-0318 | Interbody Fusion Device 7 Degree X-Large 18mm | ENDOSKELETON® TA VBR | TITAN SPINE, LLC |
30 | 00191375000037 | 2107-0220 | Interbody Fusion Device 7 Degree Large 20mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
31 | 00191375000020 | 2107-0218 | Interbody Fusion Device 7 Degree Large 18mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
32 | 00191375000013 | 2107-0120 | Interbody Fusion Device 7 Degree Standard 20mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
33 | 00191375000006 | 2107-0118 | Interbody Fusion Device 7 Degree Standard 18mm | ENDOSKELETON® TA VBR | MEDTRONIC SOFAMOR DANEK, INC. | |
34 | 00191083043272 | 38-2670-9 | 38-2670-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
35 | 00191083043265 | 38-2670-7 | 38-2670-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
36 | 00191083042695 | 38-1435-11-6C | 38-1435-11-6C | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
37 | 00191083042688 | 38-2670-17 | 38-2670-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
38 | 00191083042671 | 38-2670-15 | 38-2670-15 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
39 | 00191083042664 | 38-2670-13 | 38-2670-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
40 | 00191083042657 | 38-2670-11 | 38-2670-11 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
41 | 00191083042640 | 38-2665-9 | 38-2665-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
42 | 00191083042633 | 38-2665-7 | 38-2665-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
43 | 00191083042626 | 38-2665-17 | 38-2665-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
44 | 00191083042619 | 38-2665-15 | 38-2665-15 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
45 | 00191083042602 | 38-2665-13 | 38-2665-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
46 | 00191083042077 | 38-2250-13 | 38-2250-13 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
47 | 00191083042596 | 38-2665-11 | 38-2665-11 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
48 | 00191083042589 | 38-2660-9 | 38-2660-9 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
49 | 00191083042572 | 38-2660-7 | 38-2660-7 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |
50 | 00191083042565 | 38-2660-17 | 38-2660-17 | INTERBODY FUSION DEVICE | Cross-Fuse® II PEEK IBF System | RTI SURGICAL, INC. |