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 "NKB"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M68169102605500 6910-26-0550 6910-26-0550 5.5mm MIS Straight Rod Kit (35mm-80mm) Apelo® / Apelo® MIS ATLAS SPINE, INC.
2 M68169102408500 6910-24-0850 6910-24-0850 8.5mm Cannulated Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
3 M68169102307500 6910-23-0750 6910-23-0750 7.5mm Cannulated Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
4 M68169102206500 6910-22-0650 6910-22-0650 6.5mm Cannulated Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
5 M68169102105500 6910-21-0550 6910-21-0550 5.5mm Cannulated Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
6 M68169102004500 6910-20-0450 6910-20-0450 4.5mm Cannulated Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
7 M68169101900000 6910-19-0000 6910-19-0000 MIS Extended Head Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
8 M68169063308500 6906-33-0850 6906-33-0850 8.5mm Reduction Mono Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
9 M68169063307500 6906-33-0750 6906-33-0750 7.5mm Reduction Mono Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
10 M68169063306500 6906-33-0650 6906-33-0650 6.5mm Reduction Mono Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
11 M68169063305500 6906-33-0550 6906-33-0550 5.5mm Reduction Mono Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
12 M68169063304500 6906-33-0450 6906-33-0450 4.5mm Reduction Mono Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
13 M68169002505500 6900-25-0550 6900-25-0550 5.5mm Straight Secure Rod Kit (35mm-80mm) Apelo® / Apelo® MIS ATLAS SPINE, INC.
14 M68169001605500 6900-16-0550 6900-16-0550 5.5mm Contoured MIS Rod Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
15 M68169001505500 6900-15-0550 6900-15-0550 5.5mm Straight MIS Rod Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
16 M68169001405500 6900-14-0550 6900-14-0550 5.5mm Fixed Cross Connector Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
17 M68169001305500 6900-13-0550 6900-13-0550 5.5mm Straight Secure Rod Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
18 M68169000604500 6900-06-0450 6900-06-0450 4.5mm Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
19 M68160060900000 6006-09-0000 6006-09-0000 5.5mm Reduction Head Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
20 M68160060800000 6006-08-0000 6006-08-0000 5.5mm Standard Head Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
21 M68160060700000 6006-07-0000 6006-07-0000 Cross Connector Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
22 M68160060600000 6006-06-0000 6006-06-0000 5.5mm Contoured Rod Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
23 M68160060500000 6006-05-0000 6006-05-0000 5.5mm Straight Rod Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
24 M68160060400000 6006-04-0000 6006-04-0000 8.5mm Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
25 M68160060300000 6006-03-0000 6006-03-0000 7.5mm Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
26 M68160060200000 6006-02-0000 6006-02-0000 6.5mm Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
27 M68160060100000 6006-01-0000 6006-01-0000 5.5mm Screw Kit Apelo® / Apelo® MIS ATLAS SPINE, INC.
28 M68150100100050 5010-01-0005 5010-01-0005 Apelo® MIS Cannulated Implant Set Apelo® / Apelo® MIS ATLAS SPINE, INC.
29 M68150060300000 5006-03-0000 5006-03-0000 Apelo® Instrument Set 2 Apelo® / Apelo® MIS ATLAS SPINE, INC.
30 M68150060200000 5006-02-0000 5006-02-0000 Apelo® Instrument Set 1 Apelo® / Apelo® MIS ATLAS SPINE, INC.
31 M68150060100000 5006-01-0000 5006-01-0000 Apelo® Implant Set Apelo® / Apelo® MIS ATLAS SPINE, INC.
32 M68111101100000 1110-11-0000 1110-11-0000 MIS Flex Reduction Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
33 M68111101000000 1110-10-0000 1110-10-0000 MIS Flex Standard Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
34 M68111100900100 1110-09-0010 1110-09-0010 10mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
35 M68111100900090 1110-09-0009 1110-09-0009 9mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
36 M68111100900080 1110-09-0008 1110-09-0008 8mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
37 M68111100900070 1110-09-0007 1110-09-0007 7mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
38 M68111100900060 1110-09-0006 1110-09-0006 6mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
39 M68111100900050 1110-09-0005 1110-09-0005 5mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
40 M68111100900040 1110-09-0004 1110-09-0004 4mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
41 M68111100900030 1110-09-0003 1110-09-0003 3mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
42 M68111100900020 1110-09-0002 1110-09-0002 2mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
43 M68111100900010 1110-09-0001 1110-09-0001 1mm MIS Extended Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
44 M68111100500000 1110-05-0000 1110-05-0000 MIS Reduction Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
45 M68111100400000 1110-04-0000 1110-04-0000 MIS Standard Head Apelo® / Apelo® MIS ATLAS SPINE, INC.
46 M68111100385600 1110-03-8560 1110-03-8560 8.5mm x 60mm Cannulated Reduction Mono Screw Apelo® / Apelo® MIS ATLAS SPINE, INC.
47 M68111100385550 1110-03-8555 1110-03-8555 8.5mm x 55mm Cannulated Reduction Mono Screw Apelo® / Apelo® MIS ATLAS SPINE, INC.
48 M68111100385500 1110-03-8550 1110-03-8550 8.5mm x 50mm Cannulated Reduction Mono Screw Apelo® / Apelo® MIS ATLAS SPINE, INC.
49 M68111100385450 1110-03-8545 1110-03-8545 8.5mm x 45mm Cannulated Reduction Mono Screw Apelo® / Apelo® MIS ATLAS SPINE, INC.
50 M68111100385400 1110-03-8540 1110-03-8540 8.5mm x 40mm Cannulated Reduction Mono Screw Apelo® / Apelo® MIS ATLAS SPINE, INC.