Other products from "PRECISION SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00840019910224 26-221000-12 26-221000-12 Wide PLIF Cage Peek 0 degree 22 x 10 X 12 KWQ,MAX Appliance, Fixation, Spinal Intervertebral Body,Intervertebral Fusion Device Wit Appliance, Fixation, Spinal Intervertebral Body,Intervertebral Fusion Device With Bone Graft, Lumbar 2 ShurFit Interbody Deviceem
2 00840019926027 43-2100-00 43-2100-00 Medial Blade Rack Assembly GAD Retractor 1 MD-Max ULIF
3 00840019932684 62-BK-0103 62-BK-0103 ACIF 2C Instrument BOM ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
4 00840019932677 62-BK-0102 62-BK-0102 ACIF 2C Instrument BOM ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
5 00840019937191 39-BK-0703 39-BK-0703 Implant Kit: Std + Red (Ti) MNH,MNI Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 Implant Kit: Std + Red (Ti)
6 00840019932660 62-BK-0101 62-BK-0101 ACIF 2C Instrument BOM ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
7 00840019936972 43-8700-CA 43-8700-CA MD-Max™ Pedicle Screw System Kit MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
8 00840019936965 43-8600-CA 43-8600-CA MD-Max™ Triple Lead System Implant Case MNH,MNI Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 MD-Max ULIF
9 00840019936958 43-8500-CA 43-8500-CA MD-Max™ Implant Kit MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
10 00840019936941 43-8200-CA 43-8200-CA MD-Max™ Triple Lead MIS Instrument Kit MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
11 00840019936934 43-8100-CA 43-8100-CA MD-Max™ Triple Lead System Instrument Case MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
12 00840019936927 43-8000-CA 43-8000-CA MD-Max™ ULIF Retractor Instrument Kit MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
13 00840019932707 ACIFXX-XXP-2C-CC ACIFXX-XXP-2C-CC ACIF 2C Wide Kit Case BOM ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
14 00840019932691 62-BK-0601 62-BK-0601 ACIF 2C Wide Kit Case BOM ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
15 00840019926089 43-5000 43-5000 Lumitex Light Source LXH Orthopedic Manual Surgical Instrument 1 MD-Max ULIF
16 00840019926218 43-8700 43-8700 MD-Max™ Pedicle Screw System Case - Empty MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
17 00840019926201 43-8600 43-8600 MD-Max™ Triple Lead System Implant Tray - Empty MNH,MNI Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 MD-Max ULIF
18 00840019926195 43-8550 43-8550 MD-Max™ Implant Case - Empty MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
19 00840019926188 43-8200 43-8200 MD-Max™ Triple Lead MIS Instrument Case - Empty MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
20 00840019926171 43-8100 43-8100 MD-Max™ Triple Lead System Instrument Tray - Empty MNI,MNH Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation 2 MD-Max ULIF
21 00840019926164 43-8050 43-8050 MD-Max™ ULIF Retractor Instrument Case - Empty MNH,MNI Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 MD-Max ULIF
22 00840019926157 48-9018 48-9018 MD-Max Bottle Cap Reducer LXH Orthopedic Manual Surgical Instrument 1 MD-Max ULIF
23 00840019926140 43-6200 43-6200 Contralateral Sleeve Assembly GAD Retractor 1 MD-Max ULIF
24 00840019926133 43-6100-100 43-6100-100 Ipsilateral Sleeve Assembly, 100mm GAD Retractor 1 MD-Max ULIF
25 00840019926126 43-6100-080 43-6100-080 Ipsilateral Sleeve Assembly, 80mm GAD Retractor 1 MD-Max ULIF
26 00840019926119 43-6100-060 43-6100-060 Ipsilateral Sleeve Assembly, 60mm GAD Retractor 1 MD-Max ULIF
27 00840019926102 43-6100-040 43-6100-040 Ipsilateral Sleeve Assembly, 40mm GAD Retractor 1 MD-Max ULIF
28 00840019926096 43-6000 43-6000 Bilateral Retractor Assembly GAD Retractor 1 MD-Max ULIF
29 00840019926072 43-4100-85 43-4100-85 8.5mm MD-Max Triple Lead Tap HWX Tap, Bone 1 MD-Max ULIF
30 00840019926065 43-4100-75 43-4100-75 7.5mm MD-Max™ Triple Lead Tap HWX Tap, Bone 1 MD-Max ULIF
31 00840019926058 43-4100-65 43-4100-65 6.5mm MD-Max™ Triple Lead Tap HWX Tap, Bone 1 MD-Max ULIF
32 00840019926041 43-4100-55 43-4100-55 5.5mm MD-Max™ Triple Lead Tap HWX Tap, Bone 1 MD-Max ULIF
33 00840019926034 43-2200-00 43-2200-00 Medial Blade Bar GAD Retractor 1 MD-Max ULIF
34 00840019926010 43-2000-110 43-2000-110 Medial Retractor Blade, 110 mm GAD Retractor 1 MD-Max ULIF
35 00840019926003 43-2000-100 43-2000-100 Medial Retractor Blade, 100 mm GAD Retractor 1 MD-Max ULIF
36 00840019925990 43-2000-090 43-2000-090 Medial Retractor Blade, 90 mm GAD Retractor 1 MD-Max ULIF
37 00840019925983 43-2000-080 43-2000-080 Medial Retractor Blade, 80 mm GAD Retractor 1 MD-Max ULIF
38 00840019925976 43-2000-070 43-2000-070 Medial Retractor Blade, 70 mm GAD Retractor 1 MD-Max ULIF
39 00840019925969 43-2000-060 43-2000-060 Medial Retractor Blade, 60 mm GAD Retractor 1 MD-Max ULIF
40 00840019925952 43-2000-050 43-2000-050 Medial Retractor Blade, 50 mm GAD Retractor 1 MD-Max ULIF
41 00840019925945 43-2000-040 43-2000-040 Medial Retractor Blade, 40 mm GAD Retractor 1 MD-Max ULIF
42 00840019925938 43-1629 43-1629 Hexdriver HXX Screwdriver 1 MD-Max ULIF
43 00840019925921 43-1545 43-1545 Drill, Pedicle Targeting HTW Bit, Drill 1 MD-Max ULIF
44 00840019925907 43-0552 43-0552 Torque Limiting T-Handle 36 in-lbs LXH Orthopedic Manual Surgical Instrument 1 MD-Max ULIF
45 00840019925891 43-0080 43-0080 Reusable Light Cable-Lumitex LXH Orthopedic Manual Surgical Instrument 1 MD-Max ULIF
46 00840019921077 62-NR-5007 62-NR-5007 ACIF Rasp, 18 x 15 x 7 HTR Rasp 1 ShurFit ACIF 2C
47 00840019921428 62-TN-1815-10 62-TN-1815-10 ACIF Trial, 18 x 15 x 10 HWT Template 1 ShurFit ACIF 2C
48 00840019921060 62-NR-5006 62-NR-5006 ACIF Rasp, 18 x 15 x 6 HTR Rasp 1 ShurFit ACIF 2C
49 00840019921480 62-SC-0103 62-SC-0103 ACIF 2C Instrument Case - Expanded ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
50 00840019921473 62-SC-0102 62-SC-0102 ACIF 2C Instrument Case - Expanded + Double Wide ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 ShurFit ACIF 2C
Other products with the same Product Code "HWT"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08031497002903 SPK03Z1 InterSpace Knee Trial XL is intended to be used for the selection of the right s InterSpace Knee Trial XL is intended to be used for the selection of the right size of InterSpace Knee XL to be implanted. InterSpace Knee Trial XL TECRES SPA
2 08031497002897 SPK90Z2 InterSpace Knee ATS Trial Kit is intended to be used for the selection of the ri InterSpace Knee ATS Trial Kit is intended to be used for the selection of the right size and thickness of the InterSpace Knee ATS to be implanted. InterSpace Knee ATS Trial Kit TECRES SPA
3 08031497002880 SPC91Z1 InterSpace Hip Trial XL is intended to be used for the selection of the right si InterSpace Hip Trial XL is intended to be used for the selection of the right size of InterSpace Hip XL to be implanted. InterSpace Hip Trial XL TECRES SPA
4 08031497002873 SPC90Z1 InterSpace Hip Trial is intended to be used for the selection of the right size InterSpace Hip Trial is intended to be used for the selection of the right size of InterSpace Hip to be implanted. InterSpace Hip Trial TECRES SPA
5 08031497002866 SPC90Z3 InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem to be implanted. InterSpace Tapered Wedge Stem Trial TECRES SPA
6 08031497002347 SPK90Z1 InterSpace Knee Trial is intended to be used for the selection of the right size InterSpace Knee Trial is intended to be used for the selection of the right size of InterSpace Knee to be implanted. InterSpace Knee Trial TECRES SPA
7 08031497002323 SPC91Z3 InterSpace Tapered Wedge Stem Trial XL is intended to be used for the selection InterSpace Tapered Wedge Stem Trial XL is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem XL to be implanted. InterSpace Tapered Wedge Stem Trial XL TECRES SPA
8 08031497002040 SPS90Z1 InterSpace Shoulder Trial is intended to be used for the selection of the right InterSpace Shoulder Trial is intended to be used for the selection of the right size of InterSpace Shoulder to be implanted. InterSpace Shoulder Trial TECRES SPA
9 07640450865571 SPE-US 00 88-N SPE-US 00 88-N LATERAL RASP TRIAL 21MM H14 JULIET ® LL SPINEART SA
10 07640450865564 SPE-US 00 87-N SPE-US 00 87-N LATERAL RASP TRIAL 21MM H12 JULIET ® LL SPINEART SA
11 07640450865557 SPE-US 00 86-N SPE-US 00 86-N LATERAL RASP TRIAL 21MM H10 JULIET ® LL SPINEART SA
12 07640450865540 SPE-US 00 85-N SPE-US 00 85-N LATERAL RASP TRIAL 21MM H08 JULIET ® LL SPINEART SA
13 07640450865533 SPE-US 00 84-N SPE-US 00 84-N LATERAL RASP TRIAL 17MM H14 JULIET ® LL SPINEART SA
14 07640450865526 SPE-US 00 83-N SPE-US 00 83-N LATERAL RASP TRIAL 17MM H12 JULIET ® LL SPINEART SA
15 07640450865519 SPE-US 00 82-N SPE-US 00 82-N LATERAL RASP TRIAL 17MM H10 JULIET ® LL SPINEART SA
16 07640450865502 SPE-US 00 81-N SPE-US 00 81-N LATERAL RASP TRIAL 17MM H08 JULIET ® LL SPINEART SA
17 07640178983984 JUT-IN 05 13-N JUT-IN 05 13-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
18 07640178983977 JUT-IN 05 12-N JUT-IN 05 12-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
19 07640178983960 JUT-IN 05 11-N JUT-IN 05 11-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
20 07640178983953 JUT-IN 05 10-N JUT-IN 05 10-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
21 07640178983946 JUT-IN 05 09-N JUT-IN 05 09-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
22 07640178983939 JUT-IN 05 08-N JUT-IN 05 08-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
23 07640178983922 JUT-IN 06 16-N JUT-IN 06 16-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
24 07640178983915 JUT-IN 06 15-N JUT-IN 06 15-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
25 07640178983908 JUT-IN 06 14-N JUT-IN 06 14-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
26 07640178983892 JUT-IN 06 13-N JUT-IN 06 13-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
27 07640178983885 JUT-IN 06 12-N JUT-IN 06 12-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
28 07640185341234 SPE-IN 01 53-N SPE-IN 01 53-N Rasp Trial 14 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
29 07640185341227 SPE-IN 01 52-N SPE-IN 01 52-N Rasp Trial 12 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
30 07640185341210 SPE-IN 01 51-N SPE-IN 01 51-N Rasp Trial 10 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
31 07640185341203 SPE-IN 01 50-N SPE-IN 01 50-N Rasp Trial 08 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
32 07640185341197 SPE-IN 01 49-N SPE-IN 01 49-N Barrel – 12 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
33 07640185341180 SPE-IN 01 48-N SPE-IN 01 48-N Barrel – 12 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
34 07640185341173 SPE-IN 01 47-N SPE-IN 01 47-N Barrel – 10 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
35 07640185341166 SPE-IN 01 46-N SPE-IN 01 46-N Barrel – 08 ROMEO 2 PAD INSTRUMENTATION SPINEART SA
36 07640178988842 SPE-US 00 31-N SPE-US 00 31-N SCREW BLOCK ROMEO 2 INSTRUMENTATION SPINEART SA
37 07640178983878 JUT-IN 06 11-N JUT-IN 06 11-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
38 07640178983991 JUT-IN 05 14-N JUT-IN 05 14-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
39 07640178984028 MIS-IN 51 00-N MIS-IN 51 00-N INCISION TEMPLATE ROMEO 2 INSTRUMENTATION SPINEART SA
40 07640178984011 JUT-IN 05 16-N JUT-IN 05 16-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
41 07640178984004 JUT-IN 05 15-N JUT-IN 05 15-N TRIAL IMPLANT Ti TL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
42 07640178983861 JUT-IN 06 10-N JUT-IN 06 10-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
43 07640178983854 JUT-IN 06 09-N JUT-IN 06 09-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
44 07640178983847 JUT-IN 06 08-N JUT-IN 06 08-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
45 07640178983830 JUT-IN 06 07-N JUT-IN 06 07-N TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH JULIET ® INSTRUMENTATION SPINEART SA
46 07640178983823 JUT-IN 04 16-N JUT-IN 04 16-N TRIAL IMPLANT Ti PO/OL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
47 07640178983816 JUT-IN 04 15-N JUT-IN 04 15-N TRIAL IMPLANT Ti PO/OL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
48 07640178983809 JUT-IN 04 14-N JUT-IN 04 14-N TRIAL IMPLANT Ti PO/OL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
49 07640178983793 JUT-IN 04 13-N JUT-IN 04 13-N TRIAL IMPLANT Ti PO/OL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA
50 07640178983786 JUT-IN 04 12-N JUT-IN 04 12-N TRIAL IMPLANT Ti PO/OL SMOOTH JULIET ® INSTRUMENTATION SPINEART SA