No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00840019910224 | 26-221000-12 | 26-221000-12 | Wide PLIF Cage Peek 0 degree 22 x 10 X 12 | KWQ,MAX | Appliance, Fixation, Spinal Intervertebral Body,Intervertebral Fusion Device Wit Appliance, Fixation, Spinal Intervertebral Body,Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | ShurFit Interbody Deviceem |
2 | 00840019926027 | 43-2100-00 | 43-2100-00 | Medial Blade Rack Assembly | GAD | Retractor | 1 | MD-Max ULIF |
3 | 00840019932684 | 62-BK-0103 | 62-BK-0103 | ACIF 2C Instrument BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
4 | 00840019932677 | 62-BK-0102 | 62-BK-0102 | ACIF 2C Instrument BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
5 | 00840019937191 | 39-BK-0703 | 39-BK-0703 | Implant Kit: Std + Red (Ti) | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Implant Kit: Std + Red (Ti) |
6 | 00840019932660 | 62-BK-0101 | 62-BK-0101 | ACIF 2C Instrument BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
7 | 00840019936972 | 43-8700-CA | 43-8700-CA | MD-Max™ Pedicle Screw System Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
8 | 00840019936965 | 43-8600-CA | 43-8600-CA | MD-Max™ Triple Lead System Implant Case | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | MD-Max ULIF |
9 | 00840019936958 | 43-8500-CA | 43-8500-CA | MD-Max™ Implant Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
10 | 00840019936941 | 43-8200-CA | 43-8200-CA | MD-Max™ Triple Lead MIS Instrument Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
11 | 00840019936934 | 43-8100-CA | 43-8100-CA | MD-Max™ Triple Lead System Instrument Case | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
12 | 00840019936927 | 43-8000-CA | 43-8000-CA | MD-Max™ ULIF Retractor Instrument Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
13 | 00840019932707 | ACIFXX-XXP-2C-CC | ACIFXX-XXP-2C-CC | ACIF 2C Wide Kit Case BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
14 | 00840019932691 | 62-BK-0601 | 62-BK-0601 | ACIF 2C Wide Kit Case BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
15 | 00840019926089 | 43-5000 | 43-5000 | Lumitex Light Source | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
16 | 00840019926218 | 43-8700 | 43-8700 | MD-Max™ Pedicle Screw System Case - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
17 | 00840019926201 | 43-8600 | 43-8600 | MD-Max™ Triple Lead System Implant Tray - Empty | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | MD-Max ULIF |
18 | 00840019926195 | 43-8550 | 43-8550 | MD-Max™ Implant Case - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
19 | 00840019926188 | 43-8200 | 43-8200 | MD-Max™ Triple Lead MIS Instrument Case - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
20 | 00840019926171 | 43-8100 | 43-8100 | MD-Max™ Triple Lead System Instrument Tray - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
21 | 00840019926164 | 43-8050 | 43-8050 | MD-Max™ ULIF Retractor Instrument Case - Empty | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | MD-Max ULIF |
22 | 00840019926157 | 48-9018 | 48-9018 | MD-Max Bottle Cap Reducer | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
23 | 00840019926140 | 43-6200 | 43-6200 | Contralateral Sleeve Assembly | GAD | Retractor | 1 | MD-Max ULIF |
24 | 00840019926133 | 43-6100-100 | 43-6100-100 | Ipsilateral Sleeve Assembly, 100mm | GAD | Retractor | 1 | MD-Max ULIF |
25 | 00840019926126 | 43-6100-080 | 43-6100-080 | Ipsilateral Sleeve Assembly, 80mm | GAD | Retractor | 1 | MD-Max ULIF |
26 | 00840019926119 | 43-6100-060 | 43-6100-060 | Ipsilateral Sleeve Assembly, 60mm | GAD | Retractor | 1 | MD-Max ULIF |
27 | 00840019926102 | 43-6100-040 | 43-6100-040 | Ipsilateral Sleeve Assembly, 40mm | GAD | Retractor | 1 | MD-Max ULIF |
28 | 00840019926096 | 43-6000 | 43-6000 | Bilateral Retractor Assembly | GAD | Retractor | 1 | MD-Max ULIF |
29 | 00840019926072 | 43-4100-85 | 43-4100-85 | 8.5mm MD-Max Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
30 | 00840019926065 | 43-4100-75 | 43-4100-75 | 7.5mm MD-Max™ Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
31 | 00840019926058 | 43-4100-65 | 43-4100-65 | 6.5mm MD-Max™ Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
32 | 00840019926041 | 43-4100-55 | 43-4100-55 | 5.5mm MD-Max™ Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
33 | 00840019926034 | 43-2200-00 | 43-2200-00 | Medial Blade Bar | GAD | Retractor | 1 | MD-Max ULIF |
34 | 00840019926010 | 43-2000-110 | 43-2000-110 | Medial Retractor Blade, 110 mm | GAD | Retractor | 1 | MD-Max ULIF |
35 | 00840019926003 | 43-2000-100 | 43-2000-100 | Medial Retractor Blade, 100 mm | GAD | Retractor | 1 | MD-Max ULIF |
36 | 00840019925990 | 43-2000-090 | 43-2000-090 | Medial Retractor Blade, 90 mm | GAD | Retractor | 1 | MD-Max ULIF |
37 | 00840019925983 | 43-2000-080 | 43-2000-080 | Medial Retractor Blade, 80 mm | GAD | Retractor | 1 | MD-Max ULIF |
38 | 00840019925976 | 43-2000-070 | 43-2000-070 | Medial Retractor Blade, 70 mm | GAD | Retractor | 1 | MD-Max ULIF |
39 | 00840019925969 | 43-2000-060 | 43-2000-060 | Medial Retractor Blade, 60 mm | GAD | Retractor | 1 | MD-Max ULIF |
40 | 00840019925952 | 43-2000-050 | 43-2000-050 | Medial Retractor Blade, 50 mm | GAD | Retractor | 1 | MD-Max ULIF |
41 | 00840019925945 | 43-2000-040 | 43-2000-040 | Medial Retractor Blade, 40 mm | GAD | Retractor | 1 | MD-Max ULIF |
42 | 00840019925938 | 43-1629 | 43-1629 | Hexdriver | HXX | Screwdriver | 1 | MD-Max ULIF |
43 | 00840019925921 | 43-1545 | 43-1545 | Drill, Pedicle Targeting | HTW | Bit, Drill | 1 | MD-Max ULIF |
44 | 00840019925907 | 43-0552 | 43-0552 | Torque Limiting T-Handle 36 in-lbs | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
45 | 00840019925891 | 43-0080 | 43-0080 | Reusable Light Cable-Lumitex | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
46 | 00840019921077 | 62-NR-5007 | 62-NR-5007 | ACIF Rasp, 18 x 15 x 7 | HTR | Rasp | 1 | ShurFit ACIF 2C |
47 | 00840019921428 | 62-TN-1815-10 | 62-TN-1815-10 | ACIF Trial, 18 x 15 x 10 | HWT | Template | 1 | ShurFit ACIF 2C |
48 | 00840019921060 | 62-NR-5006 | 62-NR-5006 | ACIF Rasp, 18 x 15 x 6 | HTR | Rasp | 1 | ShurFit ACIF 2C |
49 | 00840019921480 | 62-SC-0103 | 62-SC-0103 | ACIF 2C Instrument Case - Expanded | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
50 | 00840019921473 | 62-SC-0102 | 62-SC-0102 | ACIF 2C Instrument Case - Expanded + Double Wide | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 10888857554702 | PRO-1238-16 | PRO-1238-16 | Trial Size 16x20x11 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
2 | 10888857554696 | PRO-1238-15 | PRO-1238-15 | Trial Size 16x20x10 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
3 | 10888857554689 | PRO-1238-14 | PRO-1238-14 | Trial Size 16x20x9 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
4 | 10888857554672 | PRO-1238-13 | PRO-1238-13 | Trial Size 16x20x8 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
5 | 10888857554665 | PRO-1238-12 | PRO-1238-12 | Trial Size 16x20x7 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
6 | 10888857554658 | PRO-1238-11 | PRO-1238-11 | Trial Size 16x20x6 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
7 | 10888857554641 | PRO-1238-10 | PRO-1238-10 | Trial Size 14x18x15 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
8 | 10888857554634 | PRO-1238-09 | PRO-1238-09 | Trial Size 14x18x14 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
9 | 10888857554627 | PRO-1238-08 | PRO-1238-08 | Trial Size 14x18x13 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
10 | 10888857554610 | PRO-1238-07 | PRO-1238-07 | Trial Size 14x18x12 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
11 | 10888857554603 | PRO-1238-06 | PRO-1238-06 | Trial Size 14x18x11 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
12 | 10888857554597 | PRO-1238-05 | PRO-1238-05 | Trial Size 14x18x10 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
13 | 10888857554580 | PRO-1238-04 | PRO-1238-04 | Trial Size 14x18x9 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
14 | 10888857554573 | PRO-1238-03 | PRO-1238-03 | Trial Size 14x18x8 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
15 | 10888857554566 | PRO-1238-02 | PRO-1238-02 | Trial Size 14x18x7 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
16 | 10888857554559 | PRO-1238-01 | PRO-1238-01 | Trial Size 14x18x6 mm, Convex | CASCADIA™ Interbody System | K2M, INC. |
17 | 10888857549159 | PRO-1167-02 | PRO-1167-02 | Inserter Inner Shaft | ALEUTIAN® Interbody Systems | K2M, INC. |
18 | 10888857549142 | PRO-1167-01 | PRO-1167-01 | Adjustable Inserter | ALEUTIAN® Interbody Systems | K2M, INC. |
19 | 10888857548794 | PRO-1165-02 | PRO-1165-02 | Inner Shaft | CASCADIA™ Interbody System | K2M, INC. |
20 | 10888857548763 | PRO-1161-01 | PRO-1161-01 | Trial Inserter | ALEUTIAN® Interbody Systems | K2M, INC. |
21 | 10888857528260 | PRO-1109 | PRO-1109 | Trial Inserter Size 25° | ALEUTIAN® Interbody Systems | K2M, INC. |
22 | 10888857525061 | PRO-1093-11 | PRO-1093-11 | Trial With Stop Size 12x14x15 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
23 | 10888857525054 | PRO-1093-10 | PRO-1093-10 | Trial With Stop Size 12x14x14 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
24 | 10888857525047 | PRO-1093-09 | PRO-1093-09 | Trial With Stop Size 12x14x13 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
25 | 10888857525030 | PRO-1093-08 | PRO-1093-08 | Trial With Stop Size12x14x12 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
26 | 10888857525023 | PRO-1093-07 | PRO-1093-07 | Trial With Stop Size 12x14x11 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
27 | 10888857525016 | PRO-1093-06 | PRO-1093-06 | Trial With Stop Szie 12x14x10 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
28 | 10888857525009 | PRO-1093-05 | PRO-1093-05 | Trial With Stop Size12x14x9 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
29 | 10888857524996 | PRO-1093-04 | PRO-1093-04 | Trial With Stop Size 12x14x8 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
30 | 10888857524989 | PRO-1093-03 | PRO-1093-03 | Trial With Stop Size 12x14x7 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
31 | 10888857524972 | PRO-1093-02 | PRO-1093-02 | Trial With Stop Size 12x14x6 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
32 | 10888857524965 | PRO-1093-01 | PRO-1093-01 | Trial With Stop Size 12x14x5 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
33 | 10888857524873 | PRO-1093-22 | PRO-1093-22 | Trial With Stop Size 13x16x15 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
34 | 10888857524866 | PRO-1093-21 | PRO-1093-21 | Trial With Stop Size 13x16x14 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
35 | 10888857524859 | PRO-1093-20 | PRO-1093-20 | Trial With Stop Size 13x16x13 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
36 | 10888857524842 | PRO-1093-19 | PRO-1093-19 | Trial With Stop Size 13x16x12 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
37 | 10888857524835 | PRO-1093-18 | PRO-1093-18 | Trial With Stop Size 13x16x11 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
38 | 10888857524828 | PRO-1093-17 | PRO-1093-17 | Trial With Stop Size 13x16x10 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
39 | 10888857524811 | PRO-1093-16 | PRO-1093-16 | Trial With Stop Size 13x16x9 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
40 | 10888857524804 | PRO-1093-15 | PRO-1093-15 | Trial With Stop Size 13x16x8 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
41 | 10888857524798 | PRO-1093-14 | PRO-1093-14 | Trial With Stop Size 13x16x7 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
42 | 10888857524781 | PRO-1093-13 | PRO-1093-13 | Trial With Stop Size 13x16x6 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
43 | 10888857524774 | PRO-1093-12 | PRO-1093-12 | Trial With Stop Size 13x16x5 mm, 7° | ALEUTIAN® Interbody Systems | K2M, INC. |
44 | 10888857522770 | PRO-1017 | PRO-1017 | Fixed Angle Inserter, Size 30° | ALEUTIAN® Interbody Systems | K2M, INC. |
45 | 10888857522763 | SP-4214-152 | SP-4214-152 | Trial Size 13x16x15 mm, Convex | ALEUTIAN® Interbody Systems | K2M, INC. |
46 | 10888857522756 | SP-4214-151 | SP-4214-151 | Trial Size 13x16x14 mm, Convex | ALEUTIAN® Interbody Systems | K2M, INC. |
47 | 10888857522749 | SP-4214-150 | SP-4214-150 | Trial Size 13x16x13 mm, Convex | ALEUTIAN® Interbody Systems | K2M, INC. |
48 | 10888857522732 | SP-4214-149 | SP-4214-149 | Trial Size 13x16x12 mm, Convex | ALEUTIAN® Interbody Systems | K2M, INC. |
49 | 10888857522725 | SP-4214-148 | SP-4214-148 | Trial Size 13x16x11 mm, Convex | ALEUTIAN® Interbody Systems | K2M, INC. |
50 | 10888857522718 | SP-4214-147 | SP-4214-147 | Trial Size 13x16x10 mm, Convex | ALEUTIAN® Interbody Systems | K2M, INC. |