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
1 B2215000003400 5000-00340 5000-00340 Screwdriver EPIX Anti-Rotation Cap Driver EPIX ORTHOPAEDICS INC.
2 B2215000003300 5000-00330 5000-00330 Screwdriver EPIX Distal Locking Screw Driver EPIX ORTHOPAEDICS INC.
3 B2215000002800 5000-00280 5000-00280 Screwdriver EPIX Lag Screw Compression Nut EPIX ORTHOPAEDICS INC.
4 B2215000002700 5000-00270 5000-00270 Screwdriver EPIX LAG Screw Driver EPIX ORTHOPAEDICS INC.
5 B2215000002600 5000-00260 5000-00260 Screwdriver EPIX Lag Screw Retaining Rod EPIX ORTHOPAEDICS INC.
6 B2215000000300 5000-00030 5000-00030 Screwdriver EPIX Angle Adjust Driver EPIX ORTHOPAEDICS INC.
7 B1830870000210 Panama™ 08-7000-021 AO Self Retaining Driver Panama™ FLOSPINE LLC
8 B1830870000020 Panama™ 08-7000-002 Self Retaining Driver Panama™ FLOSPINE LLC
9 B1830870000010 Panama™ 08-7000-001 Threaded Driver Panama™ FLOSPINE LLC
10 B073DRK0100200 DR-K01-0020 DR-K01-0020 SNII Screwdriver, Poly Std Assembly Kalitec Special KALITEC DIRECT LLC
11 B07311K0120240 11-K01-2024 Screwdriver, Extended Tab, Cannulated, SNI 1, Lockable, Assembly CosmoLock Pedicle Screw System KALITEC DIRECT LLC
12 B07311K0120230 11-K01-2023 Screwdriver, Extended Tab, Fixed Tap Sleeve, Assembly CosmoLock Pedicle Screw System KALITEC DIRECT LLC
13 B07311K0120220 11-K01-2022 11-K01-2022 Assembly, Screwdriver, Extended Tab Cosmolock KALITEC DIRECT LLC
14 B07311K0120210 11-K01-2021 11-K01-2021 Assembly, Screwdriver, Extended Tab, Cannulated, Lockable Cosmolock KALITEC DIRECT LLC
15 B07311K0120150 11-K01-2015 11-K01-2015 Assembly, Screwdriver, Polyaxial, Lockable Cosmolock KALITEC DIRECT LLC
16 B07311K0120140 11-K01-2014 Screwdriver, Polyaxial, Standard, Cannulated, Lockable, SNI 1 Assembly CosmoLock Pedicle Screw System KALITEC DIRECT LLC
17 B07311K0120130 11-K01-2013 Screwdriver, Polyaxial, Standard, Fixed Tap Sleeve Assembly CosmoLock Pedicle Screw System KALITEC DIRECT LLC
18 B07311K0120120 11-K01-2012 Screwdriver, Polyaxial, Standard CosmoLock Pedicle Screw System KALITEC DIRECT LLC
19 B07311K0120110 11-K01-2011 11-K01-2011 Assembly, Screwdriver, Polyaxial, Cannulated, Lockable Cosmolock KALITEC DIRECT LLC
20 B07310K0175000 10-K01-7500 Screwdriver Assembly, Tower Tab, Cannulated, SNI2 CosmoLock Pedicle Screw System KALITEC DIRECT LLC
21 B07310K0172100 10-K01-7210 10-K01-7210 Screwdriver Assembly, Tower Tab, SNI1 Cosmolock KALITEC DIRECT LLC
22 B07310K0172000 10-K01-7200 Screwdriver Assembly, Tower Tab, Cannulated SNI1 CosmoLock Pedicle Screw System KALITEC DIRECT LLC
23 B07310K0120010 10-K01-2001 Screwdriver, Tower Tab, Cannulated CosmoLock Pedicle Screw System KALITEC DIRECT LLC
24 B07308K0120000 08-K01-2000 Screw Driver, Cannulated Assembly Ocata Anterior Cervical System KALITEC DIRECT LLC
25 B064XM11504251 XM-115-0425 T-25 Standard Driver XENCO MEDICAL LLC
26 B064XM11500251 XM-115-0025 T-25 Standard Driver 1/4 Square XENCO MEDICAL LLC
27 B0621750100 1750-0100 1750-0100 Midline DTS Guide Inserter, 9-17, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
28 B06217500450 1750-0450 1750-0450 Freehand Anchor Guide, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
29 B06217500413 1750-0413 1750-0413 Anchor Driver, Triple, Angled, 19, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
30 B06217500410 1750-0410 1750-0410 Midline Anchor Guide, Angled, 19, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
31 B06217500403 1750-0403 1750-0403 Anchor Driver, Triple, Angled, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
32 B06217500402 1750-0402 1750-0402 Anchor Driver, Double, Angled, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
33 B06217500401 1750-0401 1750-0401 Anchor Driver, Single, Angled, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
34 B06217500400 1750-0400 1750-0400 Midline Anchor Guide, Angled, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
35 B06217500310 1750-0310 1750-0310 Midline Anchor Guide, Adjustable Depth Stop, 19, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
36 B06217500309 1750-0309 1750-0309 Midline Anchor Guide, 19, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
37 B06217500308 1750-0308 1750-0308 Midline Anchor Guide, Adjustable Depth Stop, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
38 B06217500307 1750-0307 1750-0307 Anchor Removal Tool, Variable Angle, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
39 B06217500306 1750-0306 1750-0306 Anchor Removal Tool, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
40 B06217500305 1750-0305 1750-00305 Anchor Removal Handle, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
41 B06217500304 1750-0304 1750-0304 SL25 MAG Driver, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
42 B06217500303 1750-0303 1750-0303 Anchor Driver, Triple, 9-17, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
43 B06217500302 1750-0302 1750-0302 Anchor Driver, Double, 9-17, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
44 B06217500301 1750-0301 1750-0301 Anchor Driver, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
45 B06217500300 1750-0300 1750-0300 Midline Anchor Guide, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
46 B06217500201 1750-0201 1750-0201 Midline Interbody Inserter Connection Shaft, Angled, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
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48 B06217500102 1750-0102 1750-0102 Midline DTS Guide Inserter, 19, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
49 B06217500101 1750-0101 1750-0101 Midline DTS Guide Inserter Connection Shaft, PISCES-SA Pisces-SA OSSEUS FUSION SYSTEMS, LLC
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