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 "NKB"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 20763000435763 559200014 SET SCREW PK 559200014 STERILE B/OFF 2PK CD Horizon™ ModuLeX™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
2 20763000435756 559200013 HEAD PK 559200013 SINGLE HEAD 4PK CD Horizon™ ModuLeX™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
3 20763000435749 559200012 HEAD PK 559200012 SINGLE HEAD 2PK CD Horizon™ ModuLeX™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
4 20763000435725 559200010 SET SCREW PK 559200010 STERILE B/OFF 4PK CD Horizon™ ModuLeX™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
5 20763000435701 559200008 MAS/SET SCREW PK 559200008 STERILE 4PK CD Horizon™ ModuLeX™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
6 20763000435695 559200007 MAS/SET SCREW PK 559200007 STERILE 2PK CD Horizon™ ModuLeX™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
7 20763000313344 5630724 SET SCREW 5630724 BRKOFF 6.0PEEK STERBX4 CD Horizon™ Astute™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
8 20763000274461 559200002 UAS/SETSCRW 559200002 5.5/6.0 STER 2PK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
9 20763000274454 559200001 MAS/SETSCRW 559200001 5.5/6.0 STER 2PK CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
10 20763000211213 6541104 PK SET SCREW 6541104 STER BREAK OFF 4PK CD HORIZON® SOLERA® VOYAGER™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
11 20763000211206 6541102 PK SET SCREW 6541102 STER BREAK OFF 2PK CD HORIZON® SOLERA® VOYAGER™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
12 20705034788354 497.789 497789 TI REPLACEMENT SETSCREWS M5 CONICAL TIP NA SYNTHES (U.S.A.) LP
13 20643169885831 6534530 SET SCREW PACK 6534530 4 PACK SET SCREW CD HORIZON® SOLERA® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
14 20643169490707 5570ROD2PER ROD 5570ROD2PER PRE-BENT 5.5X70 TI STER CD HORIZON ESSENTIALS™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
15 20643169490691 5560ROD2PER ROD 5560ROD2PER PRE-BENT 5.5X60 TI STER CD HORIZON ESSENTIALS™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
16 20643169490684 5550ROD2PER ROD 5550ROD2PER PRE-BENT 5.5X50 TI STER CD HORIZON ESSENTIALS™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
17 20643169490677 5540ROD2PER ROD 5540ROD2PER PRE-BENT 5.5X40 TI STER CD HORIZON ESSENTIALS™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
18 20643169490660 5535ROD2PER ROD 5535ROD2PER PRE-BENT 5.5X35 TI STER CD HORIZON ESSENTIALS™ Spinal System MEDTRONIC SOFAMOR DANEK, INC.
19 20643169210206 7078398 SET SCREW 7078398 5.5/6.0 TI SXT BO 4 PK CD Horizon® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
20 20643169210190 7078397 SET SCREW 7078397 5.5/6.0 TI NON BO 4 PK CD Horizon® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
21 20643169210183 7078396 SET SCREW 7078396 5.5/6.0 TI BO 4 PK CD Horizon® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
22 20613994170174 99465135 CAP 99465135 THREADED NUT CAP SI CD HORIZON® Spinal System MEDTRONIC SOFAMOR DANEK, INC.
23 18257200131952 36-5630SP 6.5MM X 30MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
24 18257200131945 36-5455SP 4.5MM X 55MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
25 18257200131938 36-5450SP 4.5MM X 50MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
26 18257200131921 36-5445SP 4.5MM X 45MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
27 18257200131914 36-5440SP 4.5MM X 40MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
28 18257200131907 36-5435SP 4.5MM X 35MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
29 18257200131891 36-5430SP 4.5MM X 30MM JANUS HA COATED FENESTRATED SCREW, SP FENESTRATED SCREWS ORTHOFIX INC.
30 18257200131884 36-4480 4.5MM X 80MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
31 18257200131877 36-4475 4.5MM X 75MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
32 18257200131860 36-4470 4.5MM X 70MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
33 18257200131853 36-4465 4.5MM X 65MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
34 18257200131846 36-4460 4.5MM X 60MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
35 18257200131839 36-4455 4.5MM X 55MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
36 18257200131822 36-4450 4.5MM X 50MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
37 18257200131815 36-4445 4.5MM X 45MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
38 18257200131808 36-4440 4.5MM X 40MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
39 18257200131792 36-4435 4.5MM X 35MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
40 18257200131785 36-4430 4.5MM X 30MM JANUS FENESTRATED SCREW FENESTRATED SCREWS ORTHOFIX INC.
41 18257200131754 36-6333 TALL ADAPTER CADDY FENESTRATED SCREWS ORTHOFIX INC.
42 18257200131747 36-6322 SHORT ADAPTER CADDY FENESTRATED SCREWS ORTHOFIX INC.
43 18257200131730 36-6321 CANNULA CADDY FENESTRATED SCREWS ORTHOFIX INC.
44 18257200131723 36-6320 BOTTOM LEVEL, JANUS FENESTRATED IMPLANT & INSTRUMENT CASE FENESTRATED SCREWS ORTHOFIX INC.
45 18257200131716 36-6316 9.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
46 18257200131709 36-6315 8.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
47 18257200131693 36-6314 7.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
48 18257200131686 36-6313 6.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
49 18257200131679 36-6312 5.5MM JANUS FENESTRATED SCREW CADDY FENESTRATED SCREWS ORTHOFIX INC.
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