Other products from "PRECISION SPINE, INC."
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
Other products with the same Product Codes "MAX, ODP, KWQ"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00813210020856 CIC2-10-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
2 00813210020849 CIC2-09-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
3 00813210020832 CIC2-08-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
4 00813210020788 CIC2-A743 Expander VariLift-C WENZEL SPINE, INC.
5 00813210020771 CIC2-A742 Retainer VariLift-C WENZEL SPINE, INC.
6 00813210020764 CIC2-A741 Inserter VariLift-C WENZEL SPINE, INC.
7 00813210020757 CIE2-A023-C01 13-15mm Extended Inserter VariLift-L WENZEL SPINE, INC.
8 00813210020740 CIE2-A022-C01 10-12mm Extended Inserter VariLift-L WENZEL SPINE, INC.
9 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
10 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
11 00813210020696 CIE3-A128 Expander, 28mm VariLift-LX WENZEL SPINE, INC.
12 00813210020689 CIE3-A124 Expander, 24mm VariLift-LX WENZEL SPINE, INC.
13 00813210020658 CIE2-A506 Extended End Cap Driver VariLift-LX WENZEL SPINE, INC.
14 00813210020641 CIE2-A505 End Cap Driver VariLift-LX WENZEL SPINE, INC.
15 00813210020566 CIE2-A218 Inserter, 10mm-12mm, Molded Handle VariLift-L WENZEL SPINE, INC.
16 00813210020559 CIE2-A217 9/11mm Retainer VariLift-L WENZEL SPINE, INC.
17 00813210020474 CIE2-A204 Reducer, Molded Handle VariLift-L WENZEL SPINE, INC.
18 00813210020467 CIE2-A203 Expander VariLift-L WENZEL SPINE, INC.
19 00813210020450 CIE2-A202 13/15mm Retainer VariLift-L WENZEL SPINE, INC.
20 00813210020443 CIE2-A201 Inserter, 13mm-15mm, Molded Handle VariLift-L WENZEL SPINE, INC.
21 00813210020436 CIE2-A028 13-15mm TR8 Extended Retainer VariLift-L WENZEL SPINE, INC.
22 00813210020429 CIE2-A027 10-12mm TR8 Extended Retainer VariLift-L WENZEL SPINE, INC.
23 00813210020412 CIE2-A026 24/28mm Extended Expander VariLift-L WENZEL SPINE, INC.
24 00813210020405 CIE2-A024 Extended Reducer, Ti Handle VariLift-L WENZEL SPINE, INC.
25 00813210020399 CIE2-A023 13-15mm Extended Inserter VariLift-L WENZEL SPINE, INC.
26 00813210020382 CIE2-A022 10-12mm Extended Inserter VariLift-L WENZEL SPINE, INC.
27 00813210020375 CIE2-A018 Retainer, 13mm-15mm VariLift-LX WENZEL SPINE, INC.
28 00813210020368 CIE2-A017 Retainer, 10mm-12mm VariLift-LX WENZEL SPINE, INC.
29 00813210020351 CIE2-A014 Reducer, Hurricane Handle VariLift-LX WENZEL SPINE, INC.
30 00813210020344 CIE2-A013 Inserter, 13mm-15mm, Hurricane Handle VariLift-LX WENZEL SPINE, INC.
31 00813210020337 CIE2-A012 Inserter, 10mm-12mm, Hurricane Handle VariLift-LX WENZEL SPINE, INC.
32 00813210020252 CIC1-A747 Removal Screwdriver VariLift-C WENZEL SPINE, INC.
33 00813210020221 CIC1-A743 Expansion Wrench VariLift-C WENZEL SPINE, INC.
34 00813210020214 CIC1-A742 Locking Wrench VariLift-C WENZEL SPINE, INC.
35 00813210020207 CIC1-A741 Insertion Wrench VariLift-C WENZEL SPINE, INC.
36 00813210020191 CIE2-A013-C01 13-15mm Inserter, with Distal Depth Marks VariLift-LX WENZEL SPINE, INC.
37 00813210020184 CIE2-A012-C01 10-12mm Inserter, with Distal Depth Marks VariLift-LX WENZEL SPINE, INC.
38 00813210020177 CIE3-15-28-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
39 00813210020160 CIE3-14-28-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
40 00813210020153 CIE3-13-28-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
41 00813210020146 CIE3-12-28-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
42 00813210020139 CIE3-11-28-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
43 00813210020122 CIE3-10-28-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
44 00813210020115 CIE3-15-24-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
45 00813210020108 CIE3-14-24-00 The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expa The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
46 00813210020092 CIE3-12-24-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
47 00813210020085 CIE3-13-24-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
48 00813210020078 CIE3-11-24-00 The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandab The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation. VariLift-LX WENZEL SPINE, INC.
49 00813210020061 CIC1-9.0-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
50 00813210020054 CIC1-7.5-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.