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 Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone Graft, Lumbar 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 Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Replacement Device 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 Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone Graft, Lumbar 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 Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Replacement Device 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 Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone Graft, Lumbar 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 Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Replacement Device 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 Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone Graft, Lumbar 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 Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Replacement Device 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 Spinal Vertebral Body Replacement Device,Intervertebral Fusion Device With Bone Graft, Lumbar 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 Intervertebral Fusion Device With Bone Graft, Lumbar,Spinal Vertebral Body Replacement Device 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 "HXX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00812258029166 SDS2-001 SDS2-001 Orthopedic surgical instrument - Screw driver, 3.5 mm, short solid PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
2 00812258029159 SDS2-000 SDS2-000 Orthopedic surgical instrument - Screw driver, 3.5 mm, short cannulated PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
3 00812258029142 SDL2-001 SDL2-001 Orthopedic surgical instrument - Screw driver, 3.5 mm, long solid PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
4 00812258029135 SDL2-000 SDL2-000 Orthopedic surgical instrument - Screw driver, 3.5 mm, long cannulated PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
5 00812258029111 LBD3-001 LBD3-001 Orthopedic surgical instrument - Straight hex driver, 6 mm PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
6 00812258029104 LBD2-001 LBD2-001 Orthopedic surgical instrument - Ball end hex driver, 6 mm PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
7 00812258028992 CRS2-000 CRS2-000 Orthopedic surgical instrument - Screw capture rod, long PRECICE® Instruments NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
8 00812258027278 SDL1-001 SDL1-001 3.5mm Hex Screw Driver, Long PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
9 00812258027261 SDL1-000 SDL1-000 Cannulated 3.5mm Hex Screw Driver, Long PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
10 00812258027254 SDS1-001 SDS1-001 3.5mm Hex Screw Driver, Short PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
11 00812258027247 SDS1-000 SDS1-000 Cannulated 3.5mm Hex Screw Driver, Short PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
12 00812258027223 RVR1-000 RVR1-000 Removal Rod PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
13 00812258027193 LBD1-000 LBD1-000 Locking Bolt Driver PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
14 00812258027032 CRS1-000 CRS1-000 Screw Capture Rod, Short PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
15 00812258027025 CRL1-000 CRL1-000 Screw Capture Rod, Long PRECICE® Trauma Nail System NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
16 00812258026936 THF3-001 THF3-001 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
17 00812258026929 THA1-000 THA1-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
18 00812258026875 DRB2-269 DRB2-269 Orthopedic Manual surgical instrument (Screw Driver) PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
19 00812258026462 THF3-000 THF3-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
20 00812258022198 THF1-000 THF1-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
21 00812258022181 THE1-000 THE1-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
22 00812258022051 DRE1-000 DRE1-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
23 00812258022044 DRD1-000 DRD1-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
24 00812258021955 THB1-000 THB1-000 Orthopedic surgical instrument (screw driver) - for use with the intramedullary Orthopedic surgical instrument (screw driver) - for use with the intramedullary limb lengthening system PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
25 00812258021849 DRB1-269 DRB1-269 Orthopedic Manual surgical instrument (Screw Driver) PRECICE® Intramedullary Limb Lengthening System Instrument NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
26 00811954013011 6041 6041 7.3mm Driver INTERVENTIONAL SPINE, INC
27 00811954012892 6029 6029 3.5/4.5mm Non-Cannulated Driver INTERVENTIONAL SPINE, INC
28 00811954012885 6028 6028 3.5/4.5mm Cannulated Driver INTERVENTIONAL SPINE, INC
29 00811954012762 6015 6015 Three Prong Driver INTERVENTIONAL SPINE, INC
30 00811954012748 6013 6013 1.9mm Driver INTERVENTIONAL SPINE, INC
31 00811954012687 6007 6007 3.5mm Nut Driver INTERVENTIONAL SPINE, INC
32 00811954012656 6004 6004 SLX Insertion Tool INTERVENTIONAL SPINE, INC
33 00811954012588 6216-00 6216-00 G3 Driver Assembly INTERVENTIONAL SPINE, INC
34 00811954012571 6215-00 6215-00 G3 Insertion Instrument INTERVENTIONAL SPINE, INC
35 00811801039942 CI-10572 Short T25 Removal Driver General Instruments ALPHATEC SPINE, INC.
36 00811801038693 CI-10379 Invictus Stab and Grab Driver - 1/4" Square Invictus ALPHATEC SPINE, INC.
37 00811801038334 CI-10400-10 Adjustable ASPIDA Driver Aspida ALPHATEC SPINE, INC.
38 00811801037979 CI-10449 Shortened T25 Retaining Driver General Instruments ALPHATEC SPINE, INC.
39 00811801037740 CI-10432 MIS Final Driver with Stop Invictus ALPHATEC SPINE, INC.
40 00811801037689 CI-10270-07 Long Set Screw Driver General Instruments ALPHATEC SPINE, INC.
41 00811801037443 CI-10369 Polyaxial Screwdriver, Locking, Stim General Instruments ALPHATEC SPINE, INC.
42 00811801037412 CI-10404 Invictus, Locking Polyaxial Driver Invictus ALPHATEC SPINE, INC.
43 00811801037405 CI-10393 T25 Screw Adjustment Driver - Fixed Handle General Instruments ALPHATEC SPINE, INC.
44 00811801037269 CI-10397 Long Invictus Locking Polyaxial Screw Driver Invictus ALPHATEC SPINE, INC.
45 00811801036958 CI-10270-06 Long Hexalobe Torque Driver General Instruments ALPHATEC SPINE, INC.
46 00811801035586 CI-10131 Angled Self-Retaining Screwdriver, 35 Degree General Instruments ALPHATEC SPINE, INC.
47 00811801035234 CI-10250 Thoracic Polyaxial Screwdriver - 1/4" Square General Instruments ALPHATEC SPINE, INC.
48 00811801035173 CI-10239 KODIAK Screwdriver - Larger Thumbwheel Kodiak ALPHATEC SPINE, INC.
49 00811801035166 CI-10242 Set Screw Driver - FD Quick Connect General Instruments ALPHATEC SPINE, INC.
50 00811801034695 CI-10186 Blade Toe Driver for LLIF Retractor Battalion ALPHATEC SPINE, INC.