Other products from "SPINEOLOGY INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M7402803015 83-02-10-15 280-3015 Rampart-O MAX Intervertebral fusion device with bone graft, lumbar 2 Rampart-O
2 M7402800023 83-04-07-29 280-0023 9x35mm Trial MAX Intervertebral fusion device with bone graft, lumbar 2 Rampart O
3 M7402800014 83-04-07-20 280-0014 10x30mm Trial MAX Intervertebral fusion device with bone graft, lumbar 2 Rampart O
4 M7405514550 10-10-80-86 551-4550 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
5 M7405514545 10-10-80-85 551-4545 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
6 M7405514540 10-10-80-84 551-4540 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
7 M7405514535 10-10-80-83 551-4535 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
8 M7405514530 10-10-80-82 551-4530 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
9 M7405514525 10-10-80-81 551-4525 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
10 M7405504550 10-10-78-42 550-4550 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
11 M7405504545 10-10-78-41 550-4545 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
12 M7405504540 10-10-78-40 550-4540 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
13 M7405504535 10-10-78-39 550-4535 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
14 M7405504530 10-10-78-38 550-4530 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
15 M7405504525 10-10-78-37 550-4525 Pedicle Screw NKB Thoracolumbosacral pedicle screw system 2 Threshold V2 Pedicle Screw
16 M7405410606 10-10-74-28 541-0606 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
17 M7405410605 10-10-74-27 541-0605 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
18 M7405410604 10-10-74-26 541-0604 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
19 M7405410506 10-10-74-25 541-0506 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
20 M7405410505 10-10-74-24 541-0505 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
21 M7405410504 10-10-74-23 541-0504 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
22 M7405410406 10-10-74-22 541-0406 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
23 M7405410405 10-10-74-21 541-0405 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
24 M7405410404 10-10-74-20 541-0404 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
25 M7405410403 10-10-74-19 541-0403 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
26 M7405410402 10-10-74-18 541-0402 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
27 M7405410306 10-10-74-17 541-0306 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
28 M7405410305 10-10-74-16 541-0305 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
29 M7405410304 10-10-74-15 541-0304 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
30 M7405410303 10-10-74-14 541-0303 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
31 M7405410302 10-10-74-13 541-0302 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
32 M7405410201 10-10-74-7 541-0201 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
33 M7405410101 10-10-74-1 541-0101 12mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
34 M7405410027 10-10-74-55 541-0027 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
35 M7405410026 10-10-74-54 541-0026 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
36 M7404905015 10-10-75-5 490-5015 Rampart One Screw OVD Intervertebral fusion device with integrated fixation, lumbar 2 Rampart One Lumbar Interbody Fusion Device
37 M7404904530 10-10-75-4 490-4530 Rampart One Screw OVD Intervertebral fusion device with integrated fixation, lumbar 2 Rampart One Lumbar Interbody Fusion Device
38 M7404904525 10-10-75-3 490-4525 Rampart One Screw OVD Intervertebral fusion device with integrated fixation, lumbar 2 Rampart One Lumbar Interbody Fusion Device
39 M7405410025 10-10-74-53 541-0025 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
40 M7405410024 10-10-74-52 541-0024 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
41 M7405410023 10-10-74-51 541-0023 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
42 M7405410022 10-10-74-50 541-0022 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
43 M7405410021 10-10-74-49 541-0021 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
44 M7405410020 10-10-74-48 541-0020 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
45 M7405410019 10-10-74-47 541-0019 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
46 M7405410018 10-10-74-46 541-0018 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
47 M7405410017 10-10-74-45 541-0017 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
48 M7405410016 10-10-74-44 541-0016 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
49 M7405410015 10-10-74-43 541-0015 10mm Elite Expandable MAX Intervertebral fusion device with bone graft, lumbar 2 Elite Expandable Interbody Fusion Device
50 M7404904520 10-10-75-2 490-4520 Rampart One Screw OVD Intervertebral fusion device with integrated fixation, lumbar 2 Rampart One Lumbar Interbody Fusion Device
Other products with the same Product Codes "MNI, NKB, MNH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00814008027552 S-01-130 Rod, Straight 5.5X130mm. The FOCUS Pedicle Screw System is intended for use in Rod, Straight 5.5X130mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
2 00814008027545 S-01-120 Rod, Straight 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in Rod, Straight 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
3 00814008027538 S-01-110 Rod, Straight 5.5X110mm. The FOCUS Pedicle Screw System is intended for use in Rod, Straight 5.5X110mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
4 00814008027521 S-01-100 Rod, Straight 5.5X100mm. The FOCUS Pedicle Screw System is intended for use in Rod, Straight 5.5X100mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
5 00814008027514 S-01-080 Rod, Straight 5.5X80mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X80mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
6 00814008027507 S-01-090 Rod, Straight 5.5X90mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X90mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
7 00814008027491 S-01-070 Rod, Straight 5.5X70mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X70mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
8 00814008027484 S-01-065 Rod, Straight 5.5X65mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X65mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
9 00814008027477 S-01-060 Rod, Straight 5.5X60mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X60mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
10 00814008027460 S-01-055 Rod, Straight 5.5X55mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X55mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
11 00814008027453 S-01-050 Rod, Straight 5.5X50mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X50mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
12 00814008027446 S-01-045 Rod, Straight 5.5X45mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X45mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
13 00814008027439 S-01-040 Rod, Straight 5.5X40mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X40mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
14 00814008027422 S-01-035 Rod, Straight 5.5X35mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X35mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
15 00814008027415 S-01-030 Rod, Straight 5.5X30mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Straight 5.5X30mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
16 00814008027408 L-01-400 Rod, Lordotic 5.5X400mm. The FOCUS Pedicle Screw System is intended for use in Rod, Lordotic 5.5X400mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00814008027392 L-01-240 Rod, Lordotic 5.5X240mm. The FOCUS Pedicle Screw System is intended for use in Rod, Lordotic 5.5X240mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00814008027385 L-01-130 Rod, Lordotic 5.5X130mm. The FOCUS Pedicle Screw System is intended for use in Rod, Lordotic 5.5X130mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00814008027378 L-01-120 Rod, Lordotic 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in Rod, Lordotic 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00814008027361 L-01-110 Rod, Lordotic 5.5X110mm. The FOCUS Pedicle Screw System is intended for use in Rod, Lordotic 5.5X110mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00814008027354 L-01-100 Rod, Lordotic 5.5X100mm. The FOCUS Pedicle Screw System is intended for use in Rod, Lordotic 5.5X100mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
22 00814008027347 L-01-080 Rod, Lordotic 5.5X80mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X80mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
23 00814008027330 L-01-090 Rod, Lordotic 5.5X90mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X90mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
24 00814008027323 L-01-070 Rod, Lordotic 5.5X70mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X70mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
25 00814008027316 L-01-065 Rod, Lordotic 5.5X65mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X65mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
26 00814008027309 L-01-050 Rod, Lordotic 5.5X50mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X50mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
27 00814008027293 L-01-060 Rod, Lordotic 5.5X60mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X60mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
28 00814008027286 L-01-050 Rod, Lordotic 5.5X55mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X55mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
29 00814008027279 L-01-045 Rod, Lordotic 5.5X45mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X45mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
30 00814008027262 L-01-040 Rod, Lordotic 5.5X40mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X40mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
31 00814008027255 L-01-035 Rod, Lordotic 5.5X35mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X35mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
32 00814008027248 L-01-030 Rod, Lordotic 5.5X30mm. The FOCUS Pedicle Screw System is intended for use in t Rod, Lordotic 5.5X30mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
33 00814008027231 PDC-850-110 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X110mm. The FOCUS Pedicle Scre PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X110mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
34 00814008027224 PDC-850-105 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X105mm. The FOCUS Pedicle Scre PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X105mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
35 00814008027217 PDC-850-100 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X100mm. The FOCUS Pedicle Scre PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X100mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
36 00814008027200 PDC-850-095 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X95mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X95mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
37 00814008027194 PDC-850-090 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X90mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X90mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
38 00814008027187 PDC-850-085 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X85mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X85mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
39 00814008027170 PDC-850-080 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X80mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X80mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
40 00814008027163 PDC-850-075 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X75mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X75mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
41 00814008027156 PDC-850-070 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X70mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X70mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
42 00814008027149 PDC-850-065 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X65mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X65mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
43 00814008027132 PDC-850-060 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X60mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X60mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
44 00814008027125 PDC-850-055 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X55mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X55mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
45 00814008027118 PDC-850-050 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X50mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X50mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
46 00814008027101 PDC-850-045 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X45mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X45mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
47 00814008027095 PDC-850-040 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X40mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X40mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
48 00814008027088 PDC-850-035 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X35mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X35mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
49 00814008027071 PDC-850-030 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X30mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X30mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
50 00814008027064 PDC-850-025 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X25mm. The FOCUS Pedicle Screw PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X25mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.