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 "HTW"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00810012483551 OL45DBS Drill bit AO QC 4.5 x 145/120mm, Sterile BIOPRO, INC.
2 00810012483544 OL35DBSL Drill bit AO QC 3.5 x 195mm, Sterile BIOPRO, INC.
3 00810012483537 OL35DBS Drill bit AO QC 3.5 x 110/85mm, Sterile BIOPRO, INC.
4 00810012483520 OL32DBS Drill bit AO QC 3.2 x 145/120mm, Sterile BIOPRO, INC.
5 00810012483490 OL28DBS Drill bit AO QC 2.8 x 110/85mm, Sterile BIOPRO, INC.
6 00810012483469 OL25DBS Drill bit AO QC 2.5 x 110/85mm, Sterile BIOPRO, INC.
7 00810012483407 OL20DBS Drill bit AO QC 2.0 x 100/75mm, Sterile BIOPRO, INC.
8 00810012483377 OL15DBS Drill bit AO QC 1.5 x 85/60mm, Sterile BIOPRO, INC.
9 00810012483230 OL11DBS Drill bit AO QC 1.1 x 85/60mm, Sterile BIOPRO, INC.
10 00810012481922 19236 CANNULATED DRILL STERILE 4.04.5MM BIOPRO, INC.
11 00810012481915 19235 CANNULATED DRILL STERILE 3.03.5MM BIOPRO, INC.
12 00810012481908 19234 CANNULATED DRILL STERILE 2.02.5MM BIOPRO, INC.
13 00810005668743 CSRW-1000T-405 Drill 4.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 4.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
14 00810005668446 HAM-1001T-DR45 Drill 4.5mm diameter cannulated instrument. The Vector Hammertoe Correction Sys Drill 4.5mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. Vector NVISION BIOMEDICAL TECHNOLOGIES, INC.
15 00810005666589 HAM-1001T-DR40 Drill 4.0mm diameter cannulated instrument. The Vector Hammertoe Correction Sys Drill 4.0mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. Vector NVISION BIOMEDICAL TECHNOLOGIES, INC.
16 00810005666572 HAM-1001T-DR35 Drill 3.5mm diameter cannulated instrument. The Vector Hammertoe Correction Sys Drill 3.5mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. Vector NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00810005665346 STK-1000T-011 Instrument: 2.5mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 2.5mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. Vertex NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00810005665339 STK-1000T-010 Instrument: 2.3mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 2.3mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. Vertex NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00810005665322 STK-1000T-009 Instrument: 2.1mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 2.1mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. Vertex NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00810005665315 STK-1000T-008 Instrument: 1.9mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 1.9mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. Vertex NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00810005665308 STK-1000T-007 Instrument: 1.7mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 1.7mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. Vertex NVISION BIOMEDICAL TECHNOLOGIES, INC.
22 00810005662727 CSRW-1000T-404 Drill 4.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 4.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
23 00810005662697 CSRW-1000T-403 Drill 3.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 3.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
24 00810005662581 TB-1000T-DR30 Instrument: Drill for 3.0mm Screw. The Javelin Tailor’s Bunion Fixation System Instrument: Drill for 3.0mm Screw. The Javelin Tailor’s Bunion Fixation System is a single-use bone fixation device intended to be permanently implanted. The system consists of a titanium alloy plate and screws that provide fixation for the 5th metatarsal. Javelin NVISION BIOMEDICAL TECHNOLOGIES, INC.
25 00810005662574 TB-1000T-DR24 Instrument: Drill for 2.4mm Screw. The Javelin Tailor’s Bunion Fixation System Instrument: Drill for 2.4mm Screw. The Javelin Tailor’s Bunion Fixation System is a single-use bone fixation device intended to be permanently implanted. The system consists of a titanium alloy plate and screws that provide fixation for the 5th metatarsal. Javelin NVISION BIOMEDICAL TECHNOLOGIES, INC.
26 00810005662468 CSRW-1000T-402 Drill 3.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 3.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
27 00810005662437 CSRW-1000T-401 Drill 2.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 2.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
28 00810005662413 CSRW-1000T-400S Solid Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bon Solid Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
29 00810005662406 CSRW-1000T-400 Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. Healix NVISION BIOMEDICAL TECHNOLOGIES, INC.
30 00810004729001 ASY-00491 ASY-00491 7.5 mm Disc Drill, FH7 NA INTEGRITY IMPLANTS INC.
31 00810004723146 ASY-00237 ASY-00237 5.0mm Cortical Drill NA INTEGRITY IMPLANTS INC.
32 00810004723139 ASY-00236 ASY-00236 4.5mm Cortical Drill NA INTEGRITY IMPLANTS INC.
33 00810004723122 ASY-00235 ASY-00235 4.0mm Cortical Drill NA INTEGRITY IMPLANTS INC.
34 00810004723115 ASY-00234 ASY-00234 3.5mm Cortical Drill NA INTEGRITY IMPLANTS INC.
35 00810004722026 ASY-00145 ASY-00145 6.5mm Disc Drill NA INTEGRITY IMPLANTS INC.
36 00763000552497 981000032 DRILL 981000032 DRILL Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
37 00763000369705 EX1119037 DRILL BIT EX1119037 12MM Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
38 00763000239879 EX0119008 DRILL BIT EX0119008 2.4MM FLUTE LESS Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
39 00763000201944 EX0918010 DRILL BIT EX0918010 SHORT 11MM Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
40 00763000152727 6975150 DRILL BIT 6975150 FLUTELESS DRILL BIT N/A MEDTRONIC SOFAMOR DANEK, INC.
41 00763000140250 5580164 TEMPLATE 5580164 ROD CURVE 5.5/6.0 NA MEDTRONIC SOFAMOR DANEK, INC.
42 00763000140205 5580154 TEMPLATE 5580154 ROD CURVE 4.75 na MEDTRONIC SOFAMOR DANEK, INC.
43 00763000078980 EX0817017 RETRACTOR EX0817017 BIOPSY DRILL Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
44 00763000078959 EX0817014 DRILL EX0817014 BIOPSY CENTER Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
45 00763000078935 EX0817012 DRILL EX0817012 CENTER Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
46 00721902725395 X0103009 ZEP DRILL BIT-TRI FLAT-300SS Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
47 00721902725364 X0103007 ZEP MONO DRILL GUIDE-300SS Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
48 00721902725357 X0103006 ZEP DUAL DRILL GUIDE-300SS Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
49 00721902566509 X0702636 CIRCULAR, 13MM DRILL BIT Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
50 00721902566493 X0702626 CIRCULAR ADJUSTABLE DRILL BIT Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.