Other products from "GENESYS ORTHOPEDICS SYSTEMS LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M719GU1000 1 GU100 Lumbar Interbody Inserter MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
2 M719GPH418M0 1 GPH1418-M 14mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
3 M719GPH2030S0 1 GPH2030-S 20mm x 30 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
4 M719GPH2030M0 1 GPH2030-M 20mm x 30 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
5 M719GPH2030L0 1 GPH2030-L 20mm x 30 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
6 M719GPH2024S0 1 GPH2024-S 20mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
7 M719GPH2024M0 1 GPH2024-M 20mm x 24 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
8 M719GPH2024L0 1 GPH2024-L 20mm x 24 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
9 M719GPH2018S0 1 GPH2018-S 20mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
10 M719GPH2018M0 1 GPH2018-M 20mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
11 M719GPH2018L0 1 GPH2018-L 20mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
12 M719GPH1830S0 1 GPH1830-S 18mm x 30 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
13 M719GPH1830M0 1 GPH1830-M 18mm x 30 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
14 M719GPH1824S0 1 GPH1824-S 18mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
15 M719GPH1824M0 1 GPH1824-M 18mm x 24 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
16 M719GPH1824L0 1 GPH1824-L 18mm x 24 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
17 M719GPH1818S0 1 GPH1818-S 18mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
18 M719GPH1818M0 1 GPH1818-M 18mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
19 M719GPH1818L0 1 GPH1818-L 18mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
20 M719GPH1630S0 1 GPH1630-S 16mm x 30 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
21 M719GPH1624S0 1 GPH1624-S 16mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
22 M719GPH1624M0 1 GPH1624-M 16mm x 24 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
23 M719GPH1618S0 1 GPH1618-S 16mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
24 M719GPH1618M0 1 GPH1618-M 16mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
25 M719GPH1618L0 1 GPH1618-L 16mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
26 M719GPH1424S0 1 GPH1424-S 14mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
27 M719GPH1418S0 1 GPH1418-S 14mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
28 M719GPH1418L0 1 GPH1418-L 14mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
29 M719GPH1218S0 1 GPH1218-S 12mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
30 M719GP8010 1 GP801 Lateral Rasp MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
31 M719GP8000 1 GP800 Lateral Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
32 M719GP5360 1 GP536 Large Angled ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
33 M719GP5350 1 GP535 Large Straight ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
34 M719GP5340 1 GP534 Small Angled ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
35 M719GP5330 1 GP533 Small Straight ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
36 M719GP53240 1 GP532-4 12in 4mm Pituitary Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
37 M719GP53220 1 GP532-2 12in 2mm Pituitary Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
38 M719GP53160 1 GP531-6 16in 6mm Kerrison Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
39 M719GP53140 1 GP531-4 16in 4mm Kerrison Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
40 M719GP5300 1 GP530 Toothless Double Action Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
41 M719GP526180 1 GP526-18 18mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
42 M719GP526160 1 GP526-16 16mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
43 M719GP526140 1 GP526-14 14mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
44 M719GP526120 1 GP526-12 12mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
45 M719GP526100 1 GP526-10 10mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
46 M719GP526080 1 GP526-08 8mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
47 M719GP3D15360 1 GP3D-1536 15mm x 36mm Parallel 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
48 M719GP3D15340 1 GP3D-1534 15mm x 34mm Parallel 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
49 M719GP3D15320 1 GP3D-1532 15mm x 32mm Parallel 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
50 M719GP3D1530C0 1 GP3D-1530C 15mm x 30mm Convex 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
Other products with the same Product Codes "KWQ, KWP, MNI, MNH, OSH, NKB"
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.