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 "HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00844588010286 0013-1-6565 0013-1-6565 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
2 00844588010279 0013-1-6560 0013-1-6560 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
3 00844588010262 0013-1-6555 0013-1-6555 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
4 00844588000447 0013-1-6550 0013-1-6550 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
5 00844588000430 0013-1-6545 0013-1-6545 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
6 00844588000423 0013-1-6540 0013-1-6540 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
7 00844588000416 0013-1-6535 0013-1-6535 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
8 00844588000409 0013-1-6530 0013-1-6530 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
9 00844588000393 0013-1-6525 0013-1-6525 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
10 00844588000386 0013-1-6520 0013-1-6520 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
11 00844588000379 0013-1-6515 0013-1-6515 Cancellous Bone Screw Consensus® Bone Screw CONSENSUS ORTHOPEDICS, INC.
12 00843575106704 8819092100 8819092100 Starter Broach b-ONE Hip Instrumentation B-ONE ORTHO, CORP.
13 00843575103949 881311641L 881311641L Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 64 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 64mm Outer Diameter, Liner Size L b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
14 00843575103932 8810003211 8810003211 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 11, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
15 00843575103925 8810003210 8810003210 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 10, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
16 00843575103918 8810003209 8810003209 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 9, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
17 00843575103901 8810003208 8810003208 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 8, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
18 00843575103895 8810003207 8810003207 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 7, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
19 00843575103888 8810003206 8810003206 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 6, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
20 00843575103871 8810003205 8810003205 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 5, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
21 00843575103864 8810003204 8810003204 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 4, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
22 00843575103857 8810003203 8810003203 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 3, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
23 00843575103840 8810003202 8810003202 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 2, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
24 00843575103833 8810003201 8810003201 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 1, Standard (132 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
25 00843575103826 8810002711 8810002711 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 11, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
26 00843575103819 8810002710 8810002710 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 10, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
27 00843575103802 8810002709 8810002709 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 9, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
28 00843575103796 8810002708 8810002708 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 8, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
29 00843575103789 8810002707 8810002707 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 7, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
30 00843575103772 8810002706 8810002706 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 6, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
31 00843575103765 8810002705 8810002705 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 5, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
32 00843575103758 8810002704 8810002704 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 4, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
33 00843575103741 8810002703 8810002703 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 3, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
34 00843575103734 8810002702 8810002702 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 2, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
35 00843575103727 8810002701 8810002701 Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; S Cementless Femoral Stem, b-ONE™ 12/14 Taper; Porous Plasma Spray + HA coating; Size 1, High (127 degree) Offset Juveno™ Femoral Hip System B-ONE ORTHO, CORP.
36 00843575103598 881311621L 881311621L Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 62 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 62mm Outer Diameter, Liner Size L b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
37 00843575103581 881311601K 881311601K Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 60m Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 60mm Outer Diameter, Liner Size K b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
38 00843575103574 881311581J 881311581J Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 58 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 58mm Outer Diameter, Liner Size J b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
39 00843575103567 881311561I 881311561I Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 56 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 56mm Outer Diameter, Liner Size I b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
40 00843575103550 881311541H 881311541H Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 5 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 54mm Outer Diameter, Liner Size H b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
41 00843575103543 881311521G 881311521G Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 5 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 52mm Outer Diameter, Liner Size G b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
42 00843575103536 881311501F 881311501F Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 5 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 50mm Outer Diameter, Liner Size F b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
43 00843575103529 881311481E 881311481E Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 48 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 48mm Outer Diameter, Liner Size E b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
44 00843575103512 881311461D 881311461D Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 4 Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 46mm Outer Diameter, Liner Size D b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
45 00843575103505 881311441C 881311441C Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 44m Cementless Acetabular Shell, Cluster Hole; Porous Plasma Spray + HA Coating; 44mm Outer Diameter, Liner Size C b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
46 00843575102621 8814006560 8814006560 Acetabular Shell Screw, 6.5mm Cancellous Bone Screw; Ti alloy; 60mm Length b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
47 00843575102614 8814006555 8814006555 Acetabular Shell Screw, 6.5mm Cancellous Bone Screw; Ti alloy; 55mm Length b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
48 00843575102607 8814006550 8814006550 Acetabular Shell Screw, 6.5mm Cancellous Bone Screw; Ti alloy; 50mm Length b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
49 00843575102591 8814006545 8814006545 Acetabular Shell Screw, 6.5mm Cancellous Bone Screw; Ti alloy; 45mm Length b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.
50 00843575102584 8814006540 8814006540 Acetabular Shell Screw, 6.5mm Cancellous Bone Screw; Ti alloy; 40mm Length b-ONE™ Primary Acetabular System B-ONE ORTHO, CORP.