Other products from "NVISION BIOMEDICAL TECHNOLOGIES, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 90814008025315 PLE-015-S PLIF Encoded 10x22 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
2 90814008024974 PLE-010-L PLIF Encoded 10x30 10mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
3 90814008024967 PLE-009-L PLIF Encoded 10x30 9mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
4 90814008024950 PLE-008-L PLIF Encoded 10x30 8mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
5 90814008024943 PLE-007-L PLIF Encoded 10x30 7mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
6 90814008024936 PLE-006-L PLIF Encoded 10x30 6mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
7 90814008024929 PLE-615-M PLIF Encoded 10x26 15mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
8 90814008024912 PLE-614-M PLIF Encoded 10x26 14mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
9 90814008024905 PLE-613-M PLIF Encoded 10x26 13mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
10 90814008024899 PLE-612-M PLIF Encoded 10x26 12mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
11 90814008024882 PLE-611-M PLIF Encoded 10x26 11mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
12 90814008024875 PLE-610-M PLIF Encoded 10x26 10mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
13 90814008024868 PLE-609-M PLIF Encoded 10x26 9mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
14 90814008024851 PLE-608-M PLIF Encoded 10x26 8mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
15 90814008024844 PLE-607-M PLIF Encoded 10x26 7mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
16 90814008024837 PLE-015-M PLIF Encoded 10x26 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
17 90814008024820 PLE-014-M PLIF Encoded 10x26 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
18 90814008024813 PLE-013-M PLIF Encoded 10x26 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
19 90814008024806 PLE-012-M PLIF Encoded 10x26 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
20 90814008024790 PLE-011-M PLIF Encoded 10x26 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
21 90814008024783 PLE-010-M PLIF Encoded 10x26 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
22 90814008024776 PLE-009-M PLIF Encoded 10x26 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
23 90814008024769 PLE-008-M PLIF Encoded 10x26 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
24 90814008024752 PLE-007-M PLIF Encoded 10x26 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
25 90814008024745 PLE-006-M PLIF Encoded 10x26 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
26 90814008024738 PLE-014-S PLIF Encoded 10x22 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
27 90814008024721 PLE-013-S PLIF Encoded 10x22 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
28 90814008024714 PLE-012-S PLIF Encoded 10x22 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
29 90814008024707 PLE-011-S PLIF Encoded 10x22 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
30 90814008024691 PLE-010-S PLIF Encoded 10x22 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
31 90814008024684 PLE-009-S PLIF Encoded 10x22 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
32 90814008024677 PLE-008-S PLIF Encoded 10x22 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
33 90814008024660 PLE-007-S PLIF Encoded 10x22 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
34 90814008024653 PLE-006-S PLIF Encoded 10x22 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
35 00810005664905 PD-1000C-750 Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 7.5 Screws. 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. LRP Tray, Surgical 1 Focus
36 00810005664899 PD-1000C-650 Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 6.5 Screws. 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. LRP Tray, Surgical 1 Focus
37 00810005662253 PD-1000C-475 Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the no Caddy 4.75 Screws. 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. LRP Tray, Surgical 1 Focus
38 00810005662246 PD-1000C-SS Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy Set Screws. 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. LRP Tray, Surgical 1 Focus
39 00810005662239 PD-1000C-CC Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non Caddy CrossLinks. 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. LRP Tray, Surgical 1 Focus
40 00810005662222 PD-1000C-LR Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Lordotic Rods. 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. LRP Tray, Surgical 1 Focus
41 00810005662215 PD-1000C-SR Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Straight Rods. 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. LRP Tray, Surgical 1 Focus
42 90814008024981 PLE-011-L PLIF Encoded 10x30 11mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
43 00810005662208 PD-1000C-106 Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 4 Instruments. 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. LRP Tray, Surgical 1 Focus
44 00810005662192 PD-1000C-105 Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 3 Instruments. 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. LRP Tray, Surgical 1 Focus
45 00810005662185 PD-1000C-104 Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 2 Instruments. 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. LRP Tray, Surgical 1 Focus
46 00810005662178 PD-1000C-103 Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 1 Instruments. 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. LRP Tray, Surgical 1 Focus
47 00810005662161 PD-1000C-102 Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for Pedicle Screw Case, Instruments. 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. LRP Tray, Surgical 1 Focus
48 00810005662154 PD-1000C-204 Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 2 INSERT 3. 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. LRP Tray, Surgical 1 Focus
49 00810005662147 PD-1000C-211 Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended Pedicle Screw Case 2 Base, Implants. 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. LRP Tray, Surgical 1 Focus
50 00810005662130 PD-1000C-202 Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 1 INSERT 2. 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. LRP Tray, Surgical 1 Focus
Other products with the same Product Code "JDR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00815432028900 7118-1814KT-C 7118-1814KT-C MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in s MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis HiMAX C CROSSROADS EXTREMITY SYSTEMS
2 00815432028894 7118-1814-C 7118-1814-C MotoCLIP/HiMAX Impant System is a Nitinol Superelastic bone staple for use in su MotoCLIP/HiMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis HiMAX C CROSSROADS EXTREMITY SYSTEMS
3 00815432028870 DynaBunion Plate 18mm Right Single Pack 7100-LP18-R The MotoBAND™ CP DynaForce® Implant System is a bone plating system indicated fo The MotoBAND™ CP DynaForce® Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® CROSSROADS EXTREMITY SYSTEMS
4 00815432028788 DynaBunion Plate 18mm Left Single Pack 7100-LP18-L The MotoBAND™ CP DynaForce® Implant System is a bone plating system indicated fo The MotoBAND™ CP DynaForce® Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® CROSSROADS EXTREMITY SYSTEMS
5 00815432028221 DynaFORCE HiMax Implant Kit, 20 x 14 x 14 7120-1414KT DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ CROSSROADS EXTREMITY SYSTEMS
6 00815432028184 DynaFORCE HiMax Implant Kit, 25 x 14 x 14 7125-1414KT DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ CROSSROADS EXTREMITY SYSTEMS
7 00815432028177 DynaFORCE HiMAX Single Packaged Implant 20mm x 18mm x 18mm 7120-1818 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
8 00815432028160 DynaFORCE HiMAX Single Packaged Implant 20mm x 18mm x 14mm 7120-1814 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
9 00815432028153 DynaFORCE HiMAX Single Packaged Implant 20mm x 16mm x 14mm 7120-1614 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
10 00815432028146 DynaFORCE HiMAX Single Packaged Implant 20mm x 14mm x 14mm 7120-1414 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
11 00815432028139 DynaFORCE HiMAX Single Packaged Implant 25mm x 18mm x 18mm 7125-1818 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
12 00815432028122 DynaFORCE HiMAX Single Packaged Implant 25mm x 18mm x 14mm 7125-1814 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
13 00815432028115 DynaFORCE HiMAX Single Packaged Implant 25mm x 16mm x 14mm 7125-1614 DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand a DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis DynaFORCE™ HiMax CROSSROADS EXTREMITY SYSTEMS
14 00815432027972 DynaForce MTP Long Plate, 5deg valgus, 10deg dorsiflexion, 25mm Clip - Left 750L-1025 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
15 00815432027965 DynaForce MTP Long Plate, 5deg valgus, 5deg dorsiflexion, 25mm Clip - Left 750L-5025 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
16 00815432027958 DynaForce MTP Long Plate, 5deg valgus, 0deg dorsiflexion, 25mm Clip - Left 750L-0025 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
17 00815432027941 DynaForce MTP Long Plate, 5deg valgus, 10deg dorsiflexion, 20mm Clip - Left 750L-1020 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
18 00815432027934 DynaForce MTP Long Plate, 5deg valgus, 5deg dorsiflexion, 20mm Clip - Left 750L-5020 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
19 00815432027927 DynaForce MTP Long Plate, 5deg valgus, 0deg dorsiflexion, 20mm Clip - Left 750L-0020 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
20 00815432027910 DynaForce MTP Long Plate, 5deg valgus, 10deg dorsiflexion, 18mm Clip - Left 750L-1018 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
21 00815432027903 DynaForce MTP Long Plate, 5deg valgus, 5deg dorsiflexion, 18mm Clip - Left 750L-5018 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
22 00815432027897 DynaForce MTP Long Plate, 5deg valgus, 0deg dorsiflexion, 18mm Clip - Left 750L-0018 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
23 00815432027880 DynaForce MTP Long Plate, 5deg valgus, 10deg dorsiflexion, 25mm Clip - Right 750R-1025 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
24 00815432027873 DynaForce MTP Long Plate, 5deg valgus, 5deg dorsiflexion, 25mm Clip - Right 750R-5025 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
25 00815432027866 DynaForce MTP Long Plate, 5deg valgus, 0deg dorsiflexion, 25mm Clip - Right 750R-0025 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
26 00815432027859 DynaForce MTP Long Plate, 5deg valgus, 10deg dorsiflexion, 20mm Clip - Right 750R-1020 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
27 00815432027842 DynaForce MTP Long Plate, 5deg valgus, 5deg dorsiflexion, 20mm Clip - Right 750R-5020 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
28 00815432027835 DynaForce MTP Long Plate, 5deg valgus, 0deg dorsiflexion, 20mm Clip - Right 750R-0020 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
29 00815432027828 DynaForce MTP Long Plate, 5deg valgus, 10deg dorsiflexion, 18mm Clip - Right 750R-1018 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
30 00815432027811 DynaForce MTP Long Plate, 5deg valgus, 5deg dorsiflexion, 18mm Clip - Right 750R-5018 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
31 00815432027804 DynaForce MTP Long Plate, 5deg valgus, 0deg dorsiflexion, 18mm Clip - Right 750R-0018 The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicate The MotoBAND™ CP DynaForce® MPJ Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System. MotoBAND™ CP DynaForce® MTP CROSSROADS EXTREMITY SYSTEMS
32 00815432027774 TriMAX Single Packaged Implant, 25mm x 22mm 7325-2222 The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
33 00815432027767 TriMAX Single Packaged Implant, 20mm x 20mm 7320-2020 The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
34 00815432027750 TriMAX Single Packaged Implant, 18mm x 22mm 7318-2222 The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
35 00815432027743 TriMAX Single Packaged Implant, 18mm x 20mm 7318-2020 The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
36 00815432027736 TriMAX Single Packaged Implant, 18mm x 18mm 7318-1818 The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
37 00815432027729 TriMAX Single Packaged Implant, 18mm x 14mm 7318-1414 The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
38 00815432027712 HiMAX Plus Single Packaged Implant, 25mm x 22mm x 22mm 7425-2222 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
39 00815432027705 HiMAX Plus Single Packaged Implant, 20mm x 20mm x 20mm 7420-2020 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
40 00815432027699 HiMAX Plus Single Packaged Implant, 18mm x 22mm x 22mm 7418-2222 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
41 00815432027682 HiMAX Plus Single Packaged Implant, 18mm x 20mm x 20mm 7418-2020 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
42 00815432027675 HiMAX Plus Single Packaged Implant, 18mm x 18mm x 18mm 7418-1818 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
43 00815432027668 HiMAX Plus Single Packaged Implant, 18mm x 18mm x 14mm 7418-1814 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
44 00815432027651 HiMAX Plus Single Packaged Implant, 18mm x 14mm x 14mm 7418-1414 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
45 00815432027644 HiMAX Plus Single Packaged Implant, 15mm x 20mm x 20mm 7415-2020 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
46 00815432027637 HiMAX Plus Single Packaged Implant, 15mm x 18mm x 18mm 7415-1818 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
47 00815432027620 HiMAX Plus Single Packaged Implant, 15mm x 15mm x 15mm 7415-1515 The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in s The HiMAX Plus Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. HiMAX Plus Implant System CROSSROADS EXTREMITY SYSTEMS
48 00815432027613 TriMAX 25mm Full Prep Kit 7300-2500KT The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
49 00815432027606 TriMAX 20mm Full Prep Kit 7300-2000KT The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surger The TriMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS
50 00815432027590 TriMAX 18mm Full Prep Kit 7300-1800KT The TriMAX Implant System is a Nitinol Superelastic bone staple for use in surge The TriMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis. TriMAX Implant System CROSSROADS EXTREMITY SYSTEMS