Other products from "MEDICAL DESIGNS LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M364119902FD90 11-9902-FD9 18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
2 M364119902FD80 11-9902-FD8 16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
3 M364119902FD70 11-9902-FD7 16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
4 M364119902FD60 11-9902-FD6 14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
5 M364119902FD40 11-9902-FD4 12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
6 M364119902FD30 11-9902-FD3 12mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 12mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
7 M364119902FD20 11-9902-FD2 10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
8 M364119902FD100 11-9902-FD10 18mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 18mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
9 M364119902FD10 11-9902-FD1 10mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 10mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar Asfora Bullet Cage® System
10 M364111109FD920 11-1109-FD9-2 Adjustable Drill Collar OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
11 M364111109FD910 11-1109-FD9-1 Drill Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
12 M364111109FD820 11-1109-FD8-2 Packing Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
13 M364111109FD810 11-1109-FD8-1 Packing Plunger OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
14 M364111109FD730 11-1109-FD7-3 Parallel Guide Sliding Block OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
15 M364111109FD720 11-1109-FD7-2 Parallel Guide Locking Nut OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
16 M364111109FD710 11-1109-FD7-1 Parallel Guide Frame OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
17 M364111109FD211 11-1109-FD21 Long Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
18 M364111109FD201 11-1109-FD20 Short Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
19 M364111109FD190 11-1109-FD19 Sterilization Case OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
20 M364111109FD180 11-1109-FD18 Drill Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
21 M364111109FD170 11-1109-FD17 Torx Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
22 M364111109FD161 11-1109-FD16 Sharp Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
23 M364111109FD150 11-1109-FD15 Plunger Distance Tool OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
24 M364111109FD140 11-1109-FD14 Cannulated Torx Driver Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
25 M364111109FD130 11-1109-FD13 Striker Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
26 M364111109FD110 11-1109-FD11 Pin Sleeve OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
27 M364111109FD100 11-1109-FD10 Drill Guide OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
28 M111109FD120 11-1109-FD12 Drill Gauge HWC,OUR Screw, Fixation, Bone,Sacroiliac Joint Fixation 2 SAMBA SCREW SYSTEM
29 M364111106FD9160 11-1106-FD9-16 16mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
30 M364111106FD9140 11-1106-FD9-14 14mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
31 M364111106FD9120 11-1106-FD9-12 12mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
32 M364111106FD8160 11-1106-FD8-16 16mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
33 M364111106FD8140 11-1106-FD8-14 14mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
34 M364111106FD8120 11-1106-FD8-12 12mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
35 M364111106FD7160 11-1106-FD7-16 16mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
36 M364111106FD7140 11-1106-FD7-14 14mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
37 M364111106FD7120 11-1106-FD7-12 12mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
38 M364111106FD4940 11-1106-FD4-94 4 Level, 94mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 94mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
39 M364111106FD4900 11-1106-FD4-90 4 Level, 90mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 90mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
40 M364111106FD4860 11-1106-FD4-86 4 Level, 86mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 86mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
41 M364111106FD4820 11-1106-FD4-82 4 Level, 82mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 82mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
42 M364111106FD4780 11-1106-FD4-78 4 Level, 78mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 78mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
43 M364111106FD4740 11-1106-FD4-74 4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
44 M364111106FD430 11-1106-FD43 Axial Driver Handle KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
45 M364111106FD420 11-1106-FD42 Axial Drill Bit Handle KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
46 M364111106FD410 11-1106-FD41 Fixed Angle Drill Guide KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
47 M364111106FD3750 11-1106-FD3-75 3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
48 M364111106FD3720 11-1106-FD3-72 3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
49 M364111106FD370 11-1106-FD37 Sterilization Case KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
50 M364111106FD3690 11-1106-FD3-69 3 Level, 69mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 69mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
Other products with the same Product Code "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10840642162110 SW19106-3016 SW19106-3016 Curved Titanium Cage - Lordotic 30 mm x 16 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
2 10840642162103 SW19106-3015 SW19106-3015 Curved Titanium Cage - Lordotic 30 mm x 15 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
3 10840642162097 SW19106-3014 SW19106-3014 Curved Titanium Cage - Lordotic 30 mm x 14 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
4 10840642162080 SW19106-3013 SW19106-3013 Curved Titanium Cage - Lordotic 30 mm x 13 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
5 10840642162073 SW19106-3012 SW19106-3012 Curved Titanium Cage - Lordotic 30 mm x 12 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
6 10840642162066 SW19106-3011 SW19106-3011 Curved Titanium Cage - Lordotic 30 mm x 11 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
7 10840642162059 SW19106-3010 SW19106-3010 Curved Titanium Cage - Lordotic 30 mm x 10 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
8 10840642162042 SW19106-3009 SW19106-3009 Curved Titanium Cage - Lordotic 30 mm x 9 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
9 10840642162035 SW19106-3008 SW19106-3008 Curved Titanium Cage - Lordotic 30 mm x 8 mm Stronghold® T 3D Titanium Interbody Device System SPINE WAVE, INC.
10 10840642161748 SW19159-2514 SW19159-2514 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
11 10840642161731 SW19159-2513 SW19159-2513 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
12 10840642161724 SW19159-2512 SW19159-2512 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
13 10840642161717 SW19159-2511 SW19159-2511 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
14 10840642161700 SW19159-2510 SW19159-2510 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
15 10840642161694 SW19159-2509 SW19159-2509 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
16 10840642161687 SW19159-2508 SW19159-2508 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
17 10840642161670 SW19159-2507 SW19159-2507 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 25 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
18 10840642161663 SW19159-2214 SW19159-2214 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
19 10840642161656 SW19159-2213 SW19159-2213 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
20 10840642161649 SW19159-2212 SW19159-2212 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
21 10840642161632 SW19159-2211 SW19159-2211 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
22 10840642161625 SW19159-2210 SW19159-2210 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
23 10840642161618 SW19159-2209 SW19159-2209 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
24 10840642161601 SW19159-2208 SW19159-2208 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
25 10840642161595 SW19159-2207 SW19159-2207 Lumbar Titanium Cage - Lordotic 15° 9.5 mm x 22 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
26 10840642161588 SW19169-3014 SW19169-3014 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
27 10840642161571 SW19169-3013 SW19169-3013 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
28 10840642161564 SW19169-3012 SW19169-3012 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
29 10840642161557 SW19169-3011 SW19169-3011 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
30 10840642161540 SW19169-3010 SW19169-3010 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
31 10840642161533 SW19169-3009 SW19169-3009 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
32 10840642161526 SW19169-3008 SW19169-3008 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
33 10840642161519 SW19169-3007 SW19169-3007 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 30 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
34 10840642161502 SW19109-3014 SW19109-3014 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
35 10840642161496 SW19109-3013 SW19109-3013 Lumbar Titanium Cage – Convex 9.5 mm x 30 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
36 10840642161489 SW19109-3012 SW19109-3012 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
37 10840642161472 SW19109-3011 SW19109-3011 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
38 10840642161465 SW19109-3010 SW19109-3010 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
39 10840642161458 SW19109-3009 SW19109-3009 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
40 10840642161441 SW19109-3008 SW19109-3008 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
41 10840642161434 SW19109-3007 SW19109-3007 Lumbar Titanium Cage - Convex 9.5 mm x 30 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
42 10840642161427 SW19169-2514 SW19169-2514 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
43 10840642161410 SW19169-2513 SW19169-2513 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 13 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
44 10840642161403 SW19169-2512 SW19169-2512 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 12 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
45 10840642161397 SW19169-2511 SW19169-2511 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 11 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
46 10840642161380 SW19169-2510 SW19169-2510 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 10 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
47 10840642161373 SW19169-2509 SW19169-2509 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 9 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
48 10840642161366 SW19169-2508 SW19169-2508 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 8 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
49 10840642161359 SW19169-2507 SW19169-2507 Lumbar Titanium Cage - Lordotic 6° 9.5 mm x 25 mm x 7 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.
50 10840642161342 SW19109-2514 SW19109-2514 Lumbar Titanium Cage - Convex 9.5 mm x 25 mm x 14 mm Stronghold® 3D Titanium Interbody Device System SPINE WAVE, INC.