Other products from "ATLAS SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M68120103900000 2010-39-0000 2010-39-0000 MIS Tissue Sleeve LXH Orthopedic Manual Surgical Instrument 1 Apelo® / Apelo® MIS
2 M681STL0170140 STL-017-014 STL-017-014 17mm Lordotic Spacer MQP,MAX Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone 2 Stature®
3 M681STL0150120 STL-015-012 STL-015-012 15mm Lordotic Spacer MAX,MQP Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Repla 2 Stature®
4 M681STL0130100 STL-013-010 STL-013-010 13mm Lordotic Spacer MQP,MAX Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone 2 Stature®
5 M681STL0110080 STL-011-008 STL-011-008 11mm Lordotic Spacer MAX,MQP Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Repla 2 Stature®
6 M681STL0090060 STL-009-006 STL-009-006 9mm Lordotic Spacer MQP,MAX Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone 2 Stature®
7 M681STF0170140 STF-017-014 STF-017-014 17mm Non-Lordotic Spacer MAX,MQP Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Repla 2 Stature®
8 M681STF0150120 STF-015-012 STF-015-012 15mm Non-Lordotic Spacer MQP,MAX Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone 2 Stature®
9 M681STF0130100 STF-013-010 STF-013-010 13mm Non-Lordotic Spacer MAX,MQP Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Repla 2 Stature®
10 M681STF0110080 STF-011-008 STF-011-008 11mm Non-Lordotic Spacer MQP,MAX Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone 2 Stature®
11 M681STF0090060 STF-009-006 STF-009-006 9mm Non-Lordotic Spacer MAX,MQP Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Repla 2 Stature®
12 M68120190900140 2019-09-0014 2019-09-0014 14mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
13 M68120190900130 2019-09-0013 2019-09-0013 13mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
14 M68120190900120 2019-09-0012 2019-09-0012 12mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
15 M68120190900110 2019-09-0011 2019-09-0011 11mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
16 M68120190900100 2019-09-0010 2019-09-0010 10mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
17 M68120190900090 2019-09-0009 2019-09-0009 9mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
18 M68120190900080 2019-09-0008 2019-09-0008 8mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
19 M68120190900070 2019-09-0007 2019-09-0007 7mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
20 M68120190800140 2019-08-0014 2019-08-0014 14mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
21 M68120190800130 2019-08-0013 2019-08-0013 13mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
22 M68120190800120 2019-08-0012 2019-08-0012 12mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
23 M68120190800110 2019-08-0011 2019-08-0011 11mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
24 M68120190800100 2019-08-0010 2019-08-0010 10mm LG Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
25 M68120190800090 2019-08-0009 2019-08-0009 9mm SM Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
26 M68120190800080 2019-08-0008 2019-08-0008 8mm SM Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
27 M68120190800070 2019-08-0007 2019-08-0007 7mm SM Lordotic Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
28 M68120190700140 2019-07-0014 2019-07-0014 14mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
29 M68120190700130 2019-07-0013 2019-07-0013 13mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
30 M68120190700120 2019-07-0012 2019-07-0012 12mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
31 M68120190700110 2019-07-0011 2019-07-0011 11mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
32 M68120190700100 2019-07-0010 2019-07-0010 10mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
33 M68120190700090 2019-07-0009 2019-07-0009 9mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
34 M68120190700080 2019-07-0008 2019-07-0008 8mm LG HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
35 M68120190600140 2019-06-0014 2019-06-0014 14mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
36 M68120190600130 2019-06-0013 2019-06-0013 13mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
37 M68120190600120 2019-06-0012 2019-06-0012 12mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
38 M68120190600110 2019-06-0011 2019-06-0011 11mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
39 M68120190600100 2019-06-0010 2019-06-0010 10mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
40 M68120190600090 2019-06-0009 2019-06-0009 9mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
41 M68120190600080 2019-06-0008 2019-06-0008 8mm SM HL Expanding Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
42 M68120190500140 2019-05-0014 2019-05-0014 14mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
43 M68120190500130 2019-05-0013 2019-05-0013 13mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
44 M68120190500120 2019-05-0012 2019-05-0012 12mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
45 M68120190500110 2019-05-0011 2019-05-0011 11mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
46 M68120190500100 2019-05-0010 2019-05-0010 10mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
47 M68120190500090 2019-05-0009 2019-05-0009 9mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
48 M68120190500080 2019-05-0008 2019-05-0008 8mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
49 M68120190500070 2019-05-0007 2019-05-0007 7mm LG Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
50 M68120190400140 2019-04-0014 2019-04-0014 14mm SM Lordotic Static Trial, HiJAK™ Cervical ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 HiJAK™ Cervical
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 FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
2 00814008027545 S-01-120 Rod, Straight 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
3 00814008027538 S-01-110 Rod, Straight 5.5X110mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
4 00814008027521 S-01-100 Rod, Straight 5.5X100mm. The FOCUS Pedicle Screw System is intended for use in 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 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 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 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 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 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 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 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 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 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 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 FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
16 00814008027408 L-01-400 Rod, Lordotic 5.5X400mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00814008027392 L-01-240 Rod, Lordotic 5.5X240mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00814008027385 L-01-130 Rod, Lordotic 5.5X130mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00814008027378 L-01-120 Rod, Lordotic 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00814008027361 L-01-110 Rod, Lordotic 5.5X110mm. The FOCUS Pedicle Screw System is intended for use in FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00814008027354 L-01-100 Rod, Lordotic 5.5X100mm. The FOCUS Pedicle Screw System is intended for use in 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 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 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 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 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 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 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 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 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 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 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 FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
33 00814008027231 PDC-850-110 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X110mm. The FOCUS Pedicle Scre FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
34 00814008027224 PDC-850-105 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X105mm. The FOCUS Pedicle Scre FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
35 00814008027217 PDC-850-100 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X100mm. The FOCUS Pedicle Scre FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
36 00814008027200 PDC-850-095 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X95mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
37 00814008027194 PDC-850-090 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X90mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
38 00814008027187 PDC-850-085 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X85mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
39 00814008027170 PDC-850-080 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X80mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
40 00814008027163 PDC-850-075 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X75mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
41 00814008027156 PDC-850-070 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X70mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
42 00814008027149 PDC-850-065 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X65mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
43 00814008027132 PDC-850-060 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X60mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
44 00814008027125 PDC-850-055 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X55mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
45 00814008027118 PDC-850-050 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X50mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
46 00814008027101 PDC-850-045 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X45mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
47 00814008027095 PDC-850-040 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X40mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
48 00814008027088 PDC-850-035 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X35mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
49 00814008027071 PDC-850-030 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X30mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
50 00814008027064 PDC-850-025 PS, MIS-Tower, Cannulated Cortical Cancellous 8.5X25mm. The FOCUS Pedicle Screw FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.