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 "LXH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 04719886892147 9404-5104 9404-5104 Stem assembly handle U2 Total Knee System UNITED ORTHOPEDIC CORP.
2 04719886892130 9404-2903 9404-2903 Tibial tower, NON-CEM, #6~#7 U2 Total Knee System UNITED ORTHOPEDIC CORP.
3 04719886892123 9404-2902 9404-2902 Tibial tower, NON-CEM, #3~#5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
4 04719886892116 9404-2901 9404-2901 Tibial tower, NON-CEM, #1~#2 U2 Total Knee System UNITED ORTHOPEDIC CORP.
5 04719886892109 9404-2612 9404-2612 Tibial drill guide, NON-CEM, Ø12.5mm U2 Total Knee System UNITED ORTHOPEDIC CORP.
6 04719886892093 9404-2611 9404-2611 Tibial drill guide, NON-CEM, Ø11.5mm U2 Total Knee System UNITED ORTHOPEDIC CORP.
7 04719886892086 9404-1301 9404-1301 Tibial punch adaptor, NON-CEM U2 Total Knee System UNITED ORTHOPEDIC CORP.
8 04719886892048 9107-6099 9107-6099 UCP Starter broach UCP Stem UNITED ORTHOPEDIC CORP.
9 04719886891997 9304-5104-RA 9304-5104-RA Ortho mallet U2 Total Knee System UNITED ORTHOPEDIC CORP.
10 04719886891034 9206-1114-RA 9206-1114-RA Universal screw driver U-Motion II UNITED ORTHOPEDIC CORP.
11 04719886891027 9206-1113-RA 9206-1113-RA Straight screw driver U-Motion II UNITED ORTHOPEDIC CORP.
12 04719886890815 9304-5111 9304-5111 Femoral A/P chamfer resection guide extractor U2 Total Knee System UNITED ORTHOPEDIC CORP.
13 04719886890792 9304-2370 9304-2370 PS Notch cutting jig, #7 U2 Total Knee System UNITED ORTHOPEDIC CORP.
14 04719886890785 9304-2360 9304-2360 PS Notch cutting jig, #6 U2 Total Knee System UNITED ORTHOPEDIC CORP.
15 04719886890778 9304-2350 9304-2350 PS Notch cutting jig, #5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
16 04719886890761 9304-2340 9304-2340 PS Notch cutting jig, #4 U2 Total Knee System UNITED ORTHOPEDIC CORP.
17 04719886890754 9304-2330 9304-2330 PS Notch cutting jig, #3 U2 Total Knee System UNITED ORTHOPEDIC CORP.
18 04719886890747 9304-2320 9304-2320 PS Notch cutting jig, #2 U2 Total Knee System UNITED ORTHOPEDIC CORP.
19 04719886890730 9304-2310 9304-2310 PS Notch cutting jig, #1 U2 Total Knee System UNITED ORTHOPEDIC CORP.
20 04719886890372 9304-2670 9304-2670 Femoral A/P chamfer resection guide, PR, #7 U2 Total Knee System UNITED ORTHOPEDIC CORP.
21 04719886890365 9304-2665 9304-2665 Femoral A/P chamfer resection guide, PR, #6.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
22 04719886890358 9304-2660 9304-2660 Femoral A/P chamfer resection guide, PR, #6 U2 Total Knee System UNITED ORTHOPEDIC CORP.
23 04719886890341 9304-2655 9304-2655 Femoral A/P chamfer resection guide, PR, #5.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
24 04719886890334 9304-2650 9304-2650 Femoral A/P chamfer resection guide, PR, #5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
25 04719886890327 9304-2645 9304-2645 Femoral A/P chamfer resection guide, PR, #4.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
26 04719886890310 9304-2640 9304-2640 Femoral A/P chamfer resection guide, PR, #4 U2 Total Knee System UNITED ORTHOPEDIC CORP.
27 04719886890303 9304-2635 9304-2635 Femoral A/P chamfer resection guide, PR, #3.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
28 04719886890297 9304-2630 9304-2630 Femoral A/P chamfer resection guide, PR, #3 U2 Total Knee System UNITED ORTHOPEDIC CORP.
29 04719886890280 9304-2625 9304-2625 Femoral A/P chamfer resection guide, PR, #2.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
30 04719886890273 9304-2620 9304-2620 Femoral A/P chamfer resection guide, PR, #2 U2 Total Knee System UNITED ORTHOPEDIC CORP.
31 04719886890266 9304-2615 9304-2615 Femoral A/P chamfer resection guide, PR, #1.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
32 04719886890259 9304-2610 9304-2610 Femoral A/P chamfer resection guide, PR, #1 U2 Total Knee System UNITED ORTHOPEDIC CORP.
33 04719886890242 9304-2470 9304-2470 Femoral A/P chamfer resection guide, AR, #7 U2 Total Knee System UNITED ORTHOPEDIC CORP.
34 04719886890235 9304-2465 9304-2465 Femoral A/P chamfer resection guide, AR, #6.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
35 04719886890228 9304-2460 9304-2460 Femoral A/P chamfer resection guide, AR, #6 U2 Total Knee System UNITED ORTHOPEDIC CORP.
36 04719886890211 9304-2455 9304-2455 Femoral A/P chamfer resection guide, AR, #5.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
37 04719886890204 9304-2450 9304-2450 Femoral A/P chamfer resection guide, AR, #5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
38 04719886890198 9304-2445 9304-2445 Femoral A/P chamfer resection guide, AR, #4.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
39 04719886890181 9304-2440 9304-2440 Femoral A/P chamfer resection guide, AR, #4 U2 Total Knee System UNITED ORTHOPEDIC CORP.
40 04719886890174 9304-2435 9304-2435 Femoral A/P chamfer resection guide, AR, #3.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
41 04719886890167 9304-2430 9304-2430 Femoral A/P chamfer resection guide, AR, #3 U2 Total Knee System UNITED ORTHOPEDIC CORP.
42 04719886890150 9304-2425 9304-2425 Femoral A/P chamfer resection guide, AR, #2.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
43 04719886890143 9304-2420 9304-2420 Femoral A/P chamfer resection guide, AR, #2 U2 Total Knee System UNITED ORTHOPEDIC CORP.
44 04719886890136 9304-2415 9304-2415 Femoral A/P chamfer resection guide, AR, #1.5 U2 Total Knee System UNITED ORTHOPEDIC CORP.
45 04719886890129 9304-2410 9304-2410 Femoral A/P chamfer resection guide, AR, #1 U2 Total Knee System UNITED ORTHOPEDIC CORP.
46 04719886890112 9304-2000-RA 9304-2000-RA Distal femoral resection guide U2 Total Knee System UNITED ORTHOPEDIC CORP.
47 04719886890105 9304-1103-RA 9304-1103-RA Universal sliding handle U2 Total Knee System UNITED ORTHOPEDIC CORP.
48 04719872179375 9301-3217 9301-3217 Head pin, 20mm UKNEE Total Knee System UNITED ORTHOPEDIC CORP.
49 04719872179368 9601-1213-RD 9601-1213-RD Universal screw driver U1™ Hip UNITED ORTHOPEDIC CORP.
50 04719872179351 9601-1213 9601-1213 Universal screw driver U1™ Hip UNITED ORTHOPEDIC CORP.