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
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No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
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2 09120069811728 680875 680875 Compression Screw, Ulna Osteotomy Plate Compression Screw I.T.S. GMBH
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5 M209201990 20199 EFFI+PRO PIN 2..6MM COIL BIOPRO, INC.
6 M209201980 20198 EFFI+PRO PIN 2.5MM COIL BIOPRO, INC.
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8 M209201960 20196 EFFI+PRO PIN 3.0MM BIOPRO, INC.
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10 M209201940 20194 EFFI+PRO PIN 2.8MM/4.5 BIOPRO, INC.
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12 M209201920 20192 EFFI+PRO COMPRESSION/DISTRACTION UNIT BIOPRO, INC.
13 M209201910 20191 EFFI+PRO RATCHET BIOPRO, INC.
14 M209201900 20190 EFFI+PRO STERILIZATION LID BIOPRO, INC.
15 M209201890 20189 EFFI+PRO STERILIZATION TRAY BIOPRO, INC.
16 M209200610 20061 Effi+Pro® Compression/Distraction Kit BIOPRO, INC.
17 08800015972994 SS0140 Perfix™ MIS U&I CORPORATION
18 08800015972970 SND0410 PERFIX DEFORMITY INSTRUMENT SYSTEM U&I CORPORATION
19 08800015972956 SND0140 PERFIX DEFORMITY INSTRUMENT SYSTEM U&I CORPORATION
20 08800015972932 SF0190 ANAX™ 5.5 SPINAL SYSTEM U&I CORPORATION
21 08800015972925 OS0180 ANAX™ OCT Spinal System U&I CORPORATION
22 08800015972918 OS0170 ANAX™ OCT Spinal System U&I CORPORATION
23 08800015960274 ISS2000 Benefix™ Interspinous Fixation System U&I CORPORATION
24 08800015959315 SZS1094 OPTIMA™ ZS Spinal System U&I CORPORATION
25 08800015959216 SZS1079 OPTIMA™ ZS Spinal System U&I CORPORATION
26 08800015959094 SZS1062 OPTIMA™ ZS Spinal System U&I CORPORATION
27 08800015959087 SZS1061 OPTIMA™ ZS Spinal System U&I CORPORATION
28 08800015958776 SZS1018 OPTIMA™ ZS Spinal System U&I CORPORATION
29 08800015956321 SFM0030 ANAX 5.5™ Spinal System U&I CORPORATION
30 08800015956314 SFM0020 ANAX 5.5™ Spinal System U&I CORPORATION
31 08800015955737 ISS1002 Benefix™ Interspinous Fixation System U&I CORPORATION
32 08800015955720 ISS1001 Benefix™ Interspinous Fixation System U&I CORPORATION
33 08800015955522 IS2020 Benefix™ Interspinous Fixation System U&I CORPORATION
34 08800015955515 IS2010 Benefix™ Interspinous Fixation System U&I CORPORATION
35 08800015953047 SN0016 Perfix™ Spinal System U&I CORPORATION
36 08800015952040 SP0016 Optima™ Spinal System U&I CORPORATION
37 08800015951241 OS0400 ANAX™ OCT System U&I CORPORATION
38 08800015951234 OS0390 ANAX™ OCT System U&I CORPORATION
39 08800015951029 OS0180 ANAX™ OCT System U&I CORPORATION
40 08800015951012 OS0170 ANAX™ OCT System U&I CORPORATION
41 08800015949804 NGS1037 Dyna Locking Trochanteric Nail U&I CORPORATION
42 08800015948623 NG0160 Dyna Locking Trochanteric Nail U&I CORPORATION
43 08800015948258 SND0410 PERFIX DEFORMITY INSTRUMENT SYSTEM U&I CORPORATION
44 08800015948104 SND0140 PERFIX DEFORMITY INSTRUMENT SYSTEM U&I CORPORATION
45 08800015947657 SS0140 Perfix™ MIS U&I CORPORATION
46 08800015947183 SFS1015 ANAX 5.5™ Spinal System U&I CORPORATION
47 08800015946919 SF0190 ANAX 5.5™ Spinal System U&I CORPORATION
48 08800015946469 SG0040 Global Spinal Fixation System™ U&I CORPORATION
49 08800015946391 SG0016 Global Spinal Fixation System™ U&I CORPORATION
50 07708604560113 0 /ST16 Inge 16,0cm SAMPEDRO INDUSTRIAS MEDICAS SAMPEDRO S A S