No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 03760219919650 | KITMC725 | NKB | Thoracolumbosacral Pedicle Screw System | 2 | STERISPINE PS | ||
2 | 03760219912026 | KITMCL535 | NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | 2 | STERISPINE PS | ||
3 | 03760219912002 | KITMCL530 | NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | 2 | STERISPINE PS | ||
4 | 03760219911517 | KITM545 | NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | 2 | STERISPINE PS | ||
5 | 03760219910787 | KITM585 | NKB | Thoracolumbosacral Pedicle Screw System | 2 | STERISPINE PS | ||
6 | 03760219910480 | KITM565 | NKB | Thoracolumbosacral Pedicle Screw System | 2 | STERISPINE PS | ||
7 | 03760219910046 | KITM540 | NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | 2 | STERISPINE PS | ||
8 | 03760219910039 | KITM535 | NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | 2 | STERISPINE PS | ||
9 | 03760219919254 | KITLCS24-07 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
10 | 03760219919247 | KITLCS24-08 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
11 | 03760219919230 | KITLCS24-09 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
12 | 03760219919223 | KITLCS24-10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
13 | 03760219919216 | KITLCS24-11 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
14 | 03760219919209 | KITLCS24-12 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
15 | 03760219919193 | KITLCS24-13 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
16 | 03760219919186 | KITLCS24-14 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
17 | 03760219919179 | KITLCS26-07 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
18 | 03760219919162 | KITLCS26-08 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
19 | 03760219919155 | KITLCS26-09 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
20 | 03760219919148 | KITLCS26-10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
21 | 03760219919131 | KITLCS26-11 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
22 | 03760219919124 | KITLCS26-12 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
23 | 03760219919117 | KITLCS26-13 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
24 | 03760219919100 | KITLCS26-14 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
25 | 03760219919094 | KITLCS30-07 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
26 | 03760219919087 | KITLCS30-08 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
27 | 03760219919070 | KITLCS30-09 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
28 | 03760219919063 | KITLCS30-10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
29 | 03760219919056 | KITLCS30-11 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
30 | 03760219919049 | KITLCS30-12 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
31 | 03760219919032 | KITLCS30-13 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
32 | 03760219919025 | KITLCS30-14 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
33 | 03760219913047 | KITANCLC 2 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
34 | 03760219912613 | KITLCS32-14 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
35 | 03760219912606 | KITLCS32-13 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
36 | 03760219912590 | KITLCS32-12 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
37 | 03760219912583 | KITLCS32-11 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
38 | 03760219912576 | KITLCS32-10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
39 | 03760219912569 | KITLCS32-09 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
40 | 03760219912552 | KITLCS32-08 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
41 | 03760219912545 | KITLCS32-07 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
42 | 03760219912538 | KITLCC32-14 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
43 | 03760219912521 | KITLCC32-13 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
44 | 03760219912514 | KITLCC32-12 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
45 | 03760219912507 | KITLCC32-11 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
46 | 03760219912491 | KITLCC32-10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
47 | 03760219912484 | KITLCC32-09 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
48 | 03760219912477 | KITLCC32-08 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
49 | 03760219912460 | KITLCC32-07 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC | ||
50 | 03760219912453 | KITLCC30-14 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | STERISPINE LC |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00887517999986 | Z200041-014 | CoRoent XL-W Trial, 14x60mm Parallel | NuVasive | NUVASIVE, INC. | |
2 | 00887517999979 | Z200041-016 | CoRoent XL-W Trial, 16x60mm Parallel | NuVasive | NUVASIVE, INC. | |
3 | 00887517999962 | Z200041-108 | CoRoent XL-W Trial, 8x60mm 10° Lordotic | NuVasive | NUVASIVE, INC. | |
4 | 00887517999955 | Z200041-110 | CoRoent XL-W Trial, 10x60mm 10° Lordotic | NuVasive | NUVASIVE, INC. | |
5 | 00887517999948 | Z200041-112 | CoRoent XL-W Trial, 12x60mm 10° Lordotic | NuVasive | NUVASIVE, INC. | |
6 | 00887517999931 | Z200041-114 | CoRoent XL-W Trial, 14x60mm 10° Lordotic | NuVasive | NUVASIVE, INC. | |
7 | 00887517999924 | Z200041-116 | CoRoent XL-W Trial, 16x60mm 10° Lordotic | NuVasive | NUVASIVE, INC. | |
8 | 00887517999917 | Z200041-208 | CoRoent XL-W Trial, 8x60mm 15° Lordotic | NuVasive | NUVASIVE, INC. | |
9 | 00887517999900 | Z200041-210 | CoRoent XL-W Trial, 10x60mm 15° Lordotic | NuVasive | NUVASIVE, INC. | |
10 | 00887517999894 | Z200041-212 | CoRoent XL-W Trial, 12x60mm 15° Lordotic | NuVasive | NUVASIVE, INC. | |
11 | 00887517999887 | Z200069-014 | CoRoent XL Trial, 14x60mm Parallel | NuVasive | NUVASIVE, INC. | |
12 | 00887517999870 | Z200069-016 | CoRoent XL Trial, 16x60mm Parallel | NuVasive | NUVASIVE, INC. | |
13 | 00887517999863 | Z200069-114 | CoRoent XL Trial, 14x60mm Lordotic | NuVasive | NUVASIVE, INC. | |
14 | 00887517999856 | Z200069-116 | CoRoent XL Trial, 16x60mm Lordotic | NuVasive | NUVASIVE, INC. | |
15 | 00887517999849 | Z200175-14 | CoRoent XL XLIF Trial Rasp, 14mm Ang | NuVasive | NUVASIVE, INC. | |
16 | 00887517999832 | Z200211 | Modulus Inserter, 15° Angled | NuVasive | NUVASIVE, INC. | |
17 | 00887517999788 | Z500116-108 | CoRoent TL Shorter Trial, 8x10x30mm 4° | NuVasive | NUVASIVE, INC. | |
18 | 00887517999771 | Z500116-110 | CoRoent TL Shorter Trial, 10x10x30mm 4° | NuVasive | NUVASIVE, INC. | |
19 | 00887517999764 | Z500116-112 | CoRoent TL Shorter Trial, 12x10x30mm 4° | NuVasive | NUVASIVE, INC. | |
20 | 00887517999757 | Z500116-114 | CoRoent TL Shorter Trial, 14x10x30mm 4° | NuVasive | NUVASIVE, INC. | |
21 | 00887517999450 | Z700163 | CoRoent Interlock Inserter - no stops | NuVasive | NUVASIVE, INC. | |
22 | 00887517999221 | Z200178-1 | CoRoent XL Angled Inserter, 20° | NuVasive | NUVASIVE, INC. | |
23 | 00887517999214 | Z200178-2 | CoRoent XL-W/XL-XW Angled Inserter, 20° | NuVasive | NUVASIVE, INC. | |
24 | 00887517998989 | Z200221-008 | CoRoent XL-W Trial Wndw, 60-8mm Par | NuVasive | NUVASIVE, INC. | |
25 | 00887517998972 | Z200221-010 | CoRoent XL-W Trial Wndw, 60-10mm Par | NuVasive | NUVASIVE, INC. | |
26 | 00887517998965 | Z200221-012 | CoRoent XL-W Trial Wndw, 60-12mm Par | NuVasive | NUVASIVE, INC. | |
27 | 00887517998958 | Z200221-014 | CoRoent XL-W Trial Wndw, 60-14mm Par | NuVasive | NUVASIVE, INC. | |
28 | 00887517998941 | Z200221-016 | CoRoent XL-W Trial Wndw, 60-16mm Par | NuVasive | NUVASIVE, INC. | |
29 | 00887517998934 | Z200221-108 | CoRoent XL-W Trial Wndw, 60-8mm 10° Lord | NuVasive | NUVASIVE, INC. | |
30 | 00887517998927 | Z200221-110 | CoRoent XL-W Trial Wndw, 60-10mm 10°Lord | NuVasive | NUVASIVE, INC. | |
31 | 00887517998910 | Z200221-112 | CoRoent XL-W Trial Wndw, 60-12mm 10°Lord | NuVasive | NUVASIVE, INC. | |
32 | 00887517998903 | Z200221-114 | CoRoent XL-W Trial Wndw, 60-14mm 10°Lord | NuVasive | NUVASIVE, INC. | |
33 | 00887517998897 | Z200221-116 | CoRoent XL-W Trial Wndw, 60-16mm 10°Lord | NuVasive | NUVASIVE, INC. | |
34 | 00887517998880 | Z200221-208 | CoRoent XL-W Trial Wndw, 60-8mm 15°Lord | NuVasive | NUVASIVE, INC. | |
35 | 00887517998873 | Z200221-210 | CoRoent XL-W Trial Wndw, 60-10mm 15°Lord | NuVasive | NUVASIVE, INC. | |
36 | 00887517998866 | Z200221-212 | CoRoent XL-W Trial Wndw, 60-12mm 15°Lord | NuVasive | NUVASIVE, INC. | |
37 | 00887517998859 | Z200222-008 | CoRoent XL Trial Wndw, 60-8mm Par | NuVasive | NUVASIVE, INC. | |
38 | 00887517998842 | Z200222-010 | CoRoent XL Trial Wndw, 60-10mm Par | NuVasive | NUVASIVE, INC. | |
39 | 00887517998835 | Z200222-012 | CoRoent XL Trial Wndw, 60-12mm Par | NuVasive | NUVASIVE, INC. | |
40 | 00887517998828 | Z200222-014 | CoRoent XL Trial Wndw, 60-14mm Par | NuVasive | NUVASIVE, INC. | |
41 | 00887517998811 | Z200222-016 | CoRoent XL Trial Wndw, 60-16mm Par | NuVasive | NUVASIVE, INC. | |
42 | 00887517998804 | Z200222-108 | CoRoent XL Trial Wndw, 60-8mm 10° Lord | NuVasive | NUVASIVE, INC. | |
43 | 00887517998798 | Z200222-110 | CoRoent XL Trial Wndw, 60-10mm 10° Lord | NuVasive | NUVASIVE, INC. | |
44 | 00887517998781 | Z200222-112 | CoRoent XL Trial Wndw, 60-12mm 10° Lord | NuVasive | NUVASIVE, INC. | |
45 | 00887517998774 | Z200222-114 | CoRoent XL Trial Wndw, 60-14mm 10° Lord | NuVasive | NUVASIVE, INC. | |
46 | 00887517998767 | Z200222-116 | CoRoent XL Trial Wndw, 60-16mm 10° Lord | NuVasive | NUVASIVE, INC. | |
47 | 00887517997814 | Z200217 | ALBINS Angled Inserter, Holed Thumbwheel | NuVasive | NUVASIVE, INC. | |
48 | 00887517997807 | Z300018 | XLR Inserter w/ Wing Tip | NuVasive | NUVASIVE, INC. | |
49 | 00887517995414 | Z200189 | Modulus Inserter for CoRoent XL | NuVasive | NUVASIVE, INC. | |
50 | 00887517995407 | Z300018-500 | XLR Angled Inserter w-Wing Tip | NuVasive | NUVASIVE, INC. |