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 05391529588656 INS-1151 INS-1151 Flexible Hex Driver Ball Tip (5mm/8mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
2 05391529582883 INS-1078 INS-1078 Long Screw Hex Driver (3.5mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
3 05391529582876 INS-1077 INS-1077 Short Screw Hex Driver (3.5mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
4 05391529582869 INS-1076 INS-1076 Short Screw Driver With Retention Hex (3.5mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
5 05391529582852 INS-1075 INS-1075 Hex Driver (5mm/8mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
6 05391529582739 INS-1060 INS-1060 Long Screw Driver With Retention Hex (3.5mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
7 05391529582722 INS-1059 INS-1059 Driver With Retention Hex (5mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
8 05391529581855 INS-1136 INS-1136 Long Removal and Insertion Hex (5mm) Apex ORTHOXEL DESIGNATED ACTIVITY COMPANY
9 05060433600883 RM06007 RM06007 AO SCREWDRIVER SPINNER (THIS PART FITS ONTO THE BOTTOM END OF "AO CANULATED SILI AO SCREWDRIVER SPINNER (THIS PART FITS ONTO THE BOTTOM END OF "AO CANULATED SILICONE SCREWDRIVER HANDLE WITH QUICK COUPLING, RM06006 - PRIMARY DI NO# (0506433600876)". THIS INSTRUMENT PART ALONG WITH "AO CANULATED SILICONE SCREWDRIVER HANDLE WITH QUICK COUPLING" MAKEUP INSTRUMENT IN630/1 - "AO CANNULATED HANDLE WITH QUICK COUPLING AND SPINNER - AS01068" LSSS LOCKDOWN MEDICAL LTD
10 05060433600876 RM06006 RM06006 AO CANNULATED SILICONE SCREWDRIVER HANDLE WITH QUICK COUPLING. THE "AO SCREWDRIV AO CANNULATED SILICONE SCREWDRIVER HANDLE WITH QUICK COUPLING. THE "AO SCREWDRIVER SPINNER" - DI NO# (05060433600883) SCREWS ONTO THE END OF THIS DEVICE. THIS CREATES THE FINAL INSTRUMENT IN630/1 - "AO CANNULATED HANDLE WITH QUICK COUPLING AND SPINNER - AS01068" LSSS LOCKDOWN MEDICAL LTD
11 05060433600777 RM04051 RM04051 AO SCREWDRIVER SHAFT Ø2.5MM (HEX). THE FINISHED PART NUMBER IS IN629/1 - "AO SCR AO SCREWDRIVER SHAFT Ø2.5MM (HEX). THE FINISHED PART NUMBER IS IN629/1 - "AO SCREWDRIVER SHAFT Ø2.5MM (HEX) - RM04051" LSSS LOCKDOWN MEDICAL LTD
12 05055662967722 OS740700-NS OS740700-NS DRIVER FOR 3.5MM SCREW, CANNULATED T15 AO QC Volition Plating System ORTHO SOLUTIONS HOLDINGS LIMITED
13 05055662963151 OS721005-NS OS721005-NS HANDLE, NON-RATCHETING CANNULATED AO QC Volition™ Plating System ORTHO SOLUTIONS HOLDINGS LIMITED
14 05055662962833 OS721010-NS OS721010-NS T10 SCREWDRIVER BIT, SELF-RETAINING Volition™ Plating System ORTHO SOLUTIONS HOLDINGS LIMITED
15 05055662956498 OS900059-NS OS900059-NS DRIVER FOR 8.0MM SCREW CANNULATED T40 JACOBS QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
16 05055662956481 OS900058-NS OS900058-NS DRIVER FOR 6.5MM SCREW CANNULATED T30 JACOBS QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
17 05055662956474 OS900057-NS OS900057-NS DRIVER FOR 5.0MM SCREW CANNULATED T20 JACOBS QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
18 05055662956467 OS900056-NS OS900056-NS DRIVER FOR 4.0MM SCREW CANNULATED T15 AO QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
19 05055662956450 OS900055-NS OS900055-NS DRIVER FOR 3.0MM SCREW CANNULATED T10 AO QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
20 05055662956443 OS900054-NS OS900054-NS DRIVER FOR 2.5MM SCREW CANNULATED T8 AO QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
21 05055662956368 OS900052-NS OS900052-NS DRIVER FOR TWIST OFF SCREW AO QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
22 05055662956078 OS900053-NS OS900053-NS DRIVER FOR 2.0MM SCREW CANNULATED T6 AO QC OrthoSolutions 'System26' Bone Screws ORTHO SOLUTIONS HOLDINGS LIMITED
23 05055662928594 OS333020 OS333020 OXFORD AFN SELF RETAINING SCREWDRIVER SHANK OXFORD ANKLE FUSION NAIL(AFN) SYSTEM ORTHO SOLUTIONS HOLDINGS LIMITED
24 05019279493937 32-467296 32-467296 AGC JIG REMOVAL INSTRUMENT BIOMET UK LTD
25 04546540756947 234-500-220 234-500-220 3.5MM HEX DRIVER NA STRYKER CORPORATION
26 04546540756350 234-020-235 234-020-235 23/28/35MM BIOSTEON SCREW DRIVER Biosteon STRYKER CORPORATION
27 04546540755827 234-020-083 234-020-083 3.5MM HEX DRIVER WITH 1.5MM CANNULATION NA STRYKER CORPORATION
28 04546540755513 234-020-035 234-020-035 23/28/35MM BIOSCREW DRIVER NA STRYKER CORPORATION
29 04546540754912 234-010-235 234-010-235 DRIVER SHAFT, TRINKLE 23/28/35MM BIOSTEON ACL SCREW NA STRYKER CORPORATION
30 04546540754646 234-010-068 234-010-068 EASY-OUT BIOABSORBABLE ACL SCREW NA STRYKER CORPORATION
31 04546540754455 234-010-035 234-010-035 DRIVER SHAFT, TRINKLE, 23/28/35MM BIOSCREW NA STRYKER CORPORATION
32 04546540259240 62-23002 62-23002 SCREWDRIVER BLADE NA STRYKER LEIBINGER GMBH & CO. KG
33 04546540255976 62-00160 62-00160 HANDLE, DENTAL SHAFT NA STRYKER LEIBINGER GMBH & CO. KG
34 EMAH10001521150 100-0152-115 100-0152-115 Humeral screw driver shaft w.Star-Bit 10=2.8mm,(f.2.7/3.5 Screws) Humeral screw driver shaft w.Star-Bit 10=2.8mm,(f.2.7/3.5 Screws) MAHE MEDICAL GMBH
35 EMAH10001520150 100-0152-015 100-0152-015 Hexalobe screw driver shaft w.Star-Bit 10=2.8mm,(f.2.7/3.5 Screws) Hexalobe screw driver shaft w.Star-Bit 10=2.8mm,(f.2.7/3.5 Screws) MAHE MEDICAL GMBH
36 04260148896712 HAT80112 HPS Screw driver for monoxial screw PARADIGM SPINE GMBH
37 04260148896705 HAT80102 HPS Polyaxial screw driver PARADIGM SPINE GMBH
38 04260148896347 HAT80300 HPS Set-Screw Driver PARADIGM SPINE GMBH
39 04260148896309 HAT80110 HPS Screw driver for monoxial screw PARADIGM SPINE GMBH
40 04260148896293 HAT80100 HPS Polyaxial screw driver PARADIGM SPINE GMBH
41 04260148893537 DAT00405 DSS™ Nut inserter PARADIGM SPINE GMBH
42 04260148893520 DAT00155 DSS™ Nut driver w/ Magazine PARADIGM SPINE GMBH
43 04260148893049 DAT00400 DSS™ Nut inserter PARADIGM SPINE GMBH
44 04260148893001 DAT00160 DSS™ Ratchet PARADIGM SPINE GMBH
45 04260148892998 DAT00150 DSS™ Nut driver PARADIGM SPINE GMBH
46 04260148890987 DAT00500 DSS™ Tray for Nut, Spacer & Washer PARADIGM SPINE GMBH
47 04260148890963 DAT00100 DSS™ Nut driver PARADIGM SPINE GMBH
48 04050435116803 27-05455 27-05455 MCD blade not self-retaining M4 AO 1 x red MONDEAL MONDEAL MEDICAL SYSTEMS GMBH
49 04050435116629 27-06255 27-06255 MCD blade M4 for 200 mm K-Wire cannulated not self-retaining AO 1 x red MONDEAL MONDEAL MEDICAL SYSTEMS GMBH
50 04050435116612 27-05355 27-05355 MCD blade not self-retaining M3 AO 1 x green MONDEAL MONDEAL MEDICAL SYSTEMS GMBH