Other products from "DIOMEDICAL CO.,LTD."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 08809263394244 A OSM00A0 Cross Link Driver MNH,KWP,MNI Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAM Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
2 08800039825269 A FA.WC.1005 Washer (CP4) D10x5 MRW SYSTEM, FACET SCREW SPINAL DEVICE U Faset
3 08809263393650 A OSM6205 Transverse Link Set 80mm KWP,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
4 08809557206802 A TI.2120 TLIF(B) Trial L38 x W11 x H16 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
5 08809557207212 A RY.PL.4106 ACP - 4-LVL PLATE 106mm KWQ Appliance, fixation, spinal intervertebral body 2 REX
6 08809557207007 A TI.2140 TLIF(B) Trial L40 x W10 x H16 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
7 08809557206147 A TI.2034 TLIF(B) Trial L28 x W10 x H10 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 IVA Cage
8 08809557206109 A TI.2030 TLIF(B) Trial L36 x W9 x H16 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
9 08809557205225 A TI.2074 TLIF(B) Trial L32 x W11 x H10 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
10 08809557205041 A TI.2086 TLIF(B) Trial L36 x W11 x H12 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
11 08809557205003 A TI.2082 TLIF(B) Trial L36 x W11 x H8 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 IVA Cage
12 08809557204457 A AL.2092 ALIF Trial L24 x W35 x A8 x H9 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 IVA Cage
13 08809489299712 A DI.2075 DLIF Trial L50 x W18 x A0 x H15 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
14 08809489299606 A DI.2042 DLIF Trial L45 x W18 x A0 x H15 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
15 08809489299569 A DI.2038 DLIF Trial L45 x W18 x A0 x H11 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
16 08809489299521 A DI.2034 DLIF Trial L45 x W18 x A0 x H7 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
17 08809489299293 A TI.2011 TLIF(B) Trial L32 x W9 x H7 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
18 08800039820554 A SO.IM.0010L Huvex 10mm PEK Spinous process plate 2 Huvex
19 08800039820530 A SO.IM.0006L Huvex 6mm PEK Spinous process plate 2 Huvex
20 08800039820332 A FA.IN.3003 Dilator Small MRW SYSTEM, FACET SCREW SPINAL DEVICE U Faset
21 08809489298876 A AC.2034 TRIAL L14 x W16 x H6 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA
22 08809489298326 A TI.0509 TLIF DISTRACTOR L28 x W9 x H15 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 IVA
23 08809489298302 A TI.0507 TLIF DISTRACTOR L28 x W9 x H13 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 IVA
24 08809489298173 A AL.0100 ALIF BONE PACKING BAR ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA
25 08809489297091 TIP.32090009 16I636 TLIF (BULLET) CAGE 32x9x0x9 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
26 08809489296995 TIP.28090009 16J549 TLIF (BULLET) CAGE 28x9x0x09 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
27 08809489295523 A FX.CD.8535 Poly Screw D type (Double) 8.5 x 35mm KWP,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
28 08809489294489 A RG.IN.0031 DRILL BIT, D4.2 MNH,KWP,MNI Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAM Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
29 08809319782971 A FX.PD.6555 Poly Screw B type (Double) 6.5 x 55mm KWP,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
30 08809263397856 A SCAI-029 ALIF Packing Bar Square ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 Galaxy
31 08809557206918 A TI.2131 TLIF(B) Trial L40 x W10 x H7 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 IVA Cage
32 08809557206901 A TI.2130 TLIF(B) Trial L40 x W9 x H16 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
33 08809263397214 A SCPI-021 PLIF Shaver 8 -021 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 Galaxy
34 08809263396699 A A123224 Galaxy ACIF cage H12 x W32 x L24 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 Galaxy
35 08809557206888 A TI.2128 TLIF(B) Trial L40 x W9 x H14 ODP,MAX Intervertebral fusion device with bone graft, cervical,Intervertebral fusion dev Intervertebral fusion device with bone graft, cervical,Intervertebral fusion device with bone graft, lumbar 2 IVA Cage
36 08809263394411 A OSM0041 Tester - Thick MNI,KWP,MNH ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Ortho ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation 2 Rexious
37 08809263394404 A OSM0040 Tester - Thin MNI,MNH,KWP ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,AP ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Rexious
38 08809263394398 A OSM0031 Probe - Straight KWP,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
39 08809263394381 A OSM0030 Probe - Curved MNH,MNI,KWP Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,AP Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Rexious
40 08809263394374 A OSM0022 Guide Pin B MNH,MNI,KWP Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,AP Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Rexious
41 08809263394367 A OSM0021 Guide Pin A KWP,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
42 08809263394350 A OSM0010 Awl MNI,KWP,MNH ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Ortho ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation 2 Rexious
43 08809263394343 A OSM00M0 Rod Fork KWP,MNI,MNH APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Ortho APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation 2 Rexious
44 08809263394336 A OSM00L0 Retractor MNH,KWP,MNI Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAM Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
45 08809263394329 A OSM00I0 Rod Holder MNI,KWP,MNH ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Ortho ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation 2 Rexious
46 08809263394312 A OSM00H0 Derotator KWP,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
47 08809263394282 A OSM00E0 Rod Pusher MNH,KWP,MNI Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAM Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 Rexious
48 08809263396064 A NC651514 Galaxy ACIF cage H6 x W15 x L14 MAX,ODP Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with bone graft, cervical 2 Galaxy
49 08809263394947 A SH.AL.0007 Left Angled Hook - 7mm .F KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Rexious HOOK
50 08809263394930 A SH.AL.0005 Left Angled Hook - 5mm .F KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 Rexious HOOK
Other products with the same Product Code "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.