Other products from "ZIMMER TRABECULAR METAL TECHNOLOGY INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024464315 00-7050-078-00 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
2 00889024464292 00-7050-076-00 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
3 00889024464278 00-7050-038-00 HWR DRIVER, PROSTHESIS 1 NA
4 00889024464261 00-7050-036-00 HWR DRIVER, PROSTHESIS 1 NA
5 00889024464254 00-7361-052-22 HXB PROBE 1 NA
6 00889024464247 00-7360-070-28 HXB PROBE 1 NA
7 00889024464230 00-7360-068-28 HXB PROBE 1 NA
8 00889024464223 00-7360-066-28 HXB PROBE 1 NA
9 00889024464216 00-7360-064-28 HXB PROBE 1 NA
10 00889024464209 00-7360-062-28 HXB PROBE 1 NA
11 00889024464193 00-7360-060-28 HXB PROBE 1 NA
12 00889024464186 00-7360-058-28 HXB PROBE 1 NA
13 00889024464179 00-7360-056-28 HXB PROBE 1 NA
14 00889024464162 00-7360-054-28 HXB PROBE 1 NA
15 00889024464155 00-7360-052-28 HXB PROBE 1 NA
16 00889024320635 96-701-30001 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
17 00889024320628 96-701-21161 96-701-21161 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
18 00889024320611 96-701-21121 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
19 00889024320604 96-701-21101 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
20 00889024320598 96-701-21081 96-701-21081 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
21 00889024320581 96-701-20161 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
22 00889024320574 96-701-20121 96-701-20121 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
23 00889024320567 96-701-20101 96-701-20101 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
24 00889024320550 96-701-20081 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
25 00889024320543 96-701-10001 96-701-10001 MAX Intervertebral fusion device with bone graft, lumbar 2 TM Ardis®
26 00889024320536 96-499-60001 96-499-60001 FSM,MQP,MAX TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebr TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 1 NA
27 00889024320529 96-499-50001 96-499-50001 MQP,MAX,FSM SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT 1 NA
28 00889024320512 96-499-40001 96-499-40001 MQP,MAX,FSM SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT 1 NA
29 00889024320505 96-499-30001 96-499-30001 MAX,MQP,FSM Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT 1 NA
30 00889024320499 96-499-20001 96-499-20001 MQP,MAX,FSM SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT 1 NA
31 00889024320482 96-499-10001 96-499-10001 MQP,FSM,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebr SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebral fusion device with bone graft, lumbar 1 NA
32 00889024320031 96-215-21031 96-215-21031 GAD RETRACTOR 1 NA
33 00889024320024 96-215-21021 96-215-21021 GAD RETRACTOR 1 NA
34 00889024320017 96-215-21011 96-215-21011 GAD RETRACTOR 1 NA
35 00889024320000 96-215-21001 96-215-21001 GAD RETRACTOR 1 NA
36 00889024319998 96-215-20001 96-215-20001 GAD RETRACTOR 1 NA
37 00889024319981 96-215-19011 96-215-19011 GAD RETRACTOR 1 NA
38 00889024319974 96-215-19001 96-215-19001 GAD RETRACTOR 1 NA
39 00889024319967 96-215-18001 96-215-18001 GAD RETRACTOR 1 NA
40 00889024319950 96-215-17011 96-215-17011 GAD RETRACTOR 1 NA
41 00889024319943 96-215-17001 96-215-17001 GAD RETRACTOR 1 NA
42 00889024319936 96-215-16001 96-215-16001 GAD RETRACTOR 1 NA
43 00889024319929 96-215-15011 96-215-15011 GAD RETRACTOR 1 NA
44 00889024319912 96-215-15001 96-215-15001 GAD RETRACTOR 1 NA
45 00889024319905 96-215-14011 96-215-14011 GAD RETRACTOR 1 NA
46 00889024319899 96-215-14001 96-215-14001 GAD RETRACTOR 1 NA
47 00889024319882 96-215-13011 96-215-13011 GAD RETRACTOR 1 NA
48 00889024319875 96-215-13001 96-215-13001 GAD RETRACTOR 1 NA
49 00889024319868 96-215-12011 96-215-12011 GAD RETRACTOR 1 NA
50 00889024319851 96-215-12001 96-215-12001 GAD RETRACTOR 1 NA
Other products with the same Product Code "HTW"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00810012485302 19734 CANNULATED DRILL 6.5MM BIOPRO, INC.
2 00810012485296 19142 CANNULATED DRILL 4.04.5MM BIOPRO, INC.
3 00810012485272 18333 CANNULATED DRILL 3.03.5MM BIOPRO, INC.
4 00810012485111 INS003 Drill bit with graduations Ø 4.5mm, Sterile BIOPRO, INC.
5 00810012483551 OL45DBS Drill bit AO QC 4.5 x 145/120mm, Sterile BIOPRO, INC.
6 00810012483544 OL35DBSL Drill bit AO QC 3.5 x 195mm, Sterile BIOPRO, INC.
7 00810012483537 OL35DBS Drill bit AO QC 3.5 x 110/85mm, Sterile BIOPRO, INC.
8 00810012483520 OL32DBS Drill bit AO QC 3.2 x 145/120mm, Sterile BIOPRO, INC.
9 00810012483490 OL28DBS Drill bit AO QC 2.8 x 110/85mm, Sterile BIOPRO, INC.
10 00810012483469 OL25DBS Drill bit AO QC 2.5 x 110/85mm, Sterile BIOPRO, INC.
11 00810012483407 OL20DBS Drill bit AO QC 2.0 x 100/75mm, Sterile BIOPRO, INC.
12 00810012483377 OL15DBS Drill bit AO QC 1.5 x 85/60mm, Sterile BIOPRO, INC.
13 00810012483230 OL11DBS Drill bit AO QC 1.1 x 85/60mm, Sterile BIOPRO, INC.
14 00810012481922 19236 CANNULATED DRILL STERILE 4.04.5MM BIOPRO, INC.
15 00810012481915 19235 CANNULATED DRILL STERILE 3.03.5MM BIOPRO, INC.
16 00810012481908 19234 CANNULATED DRILL STERILE 2.02.5MM BIOPRO, INC.
17 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.
18 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.
19 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.
20 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.
21 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.
22 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.
23 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.
24 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.
25 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.
26 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.
27 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.
28 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.
29 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.
30 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.
31 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.
32 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.
33 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.
34 00810004729001 ASY-00491 ASY-00491 7.5 mm Disc Drill, FH7 NA INTEGRITY IMPLANTS INC.
35 00810004723146 ASY-00237 ASY-00237 5.0mm Cortical Drill NA INTEGRITY IMPLANTS INC.
36 00810004723139 ASY-00236 ASY-00236 4.5mm Cortical Drill NA INTEGRITY IMPLANTS INC.
37 00810004723122 ASY-00235 ASY-00235 4.0mm Cortical Drill NA INTEGRITY IMPLANTS INC.
38 00810004723115 ASY-00234 ASY-00234 3.5mm Cortical Drill NA INTEGRITY IMPLANTS INC.
39 00810004722026 ASY-00145 ASY-00145 6.5mm Disc Drill NA INTEGRITY IMPLANTS INC.
40 00763000552497 981000032 DRILL 981000032 DRILL Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
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42 00763000239879 EX0119008 DRILL BIT EX0119008 2.4MM FLUTE LESS Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
43 00763000201944 EX0918010 DRILL BIT EX0918010 SHORT 11MM Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
44 00763000152727 6975150 DRILL BIT 6975150 FLUTELESS DRILL BIT N/A MEDTRONIC SOFAMOR DANEK, INC.
45 00763000140250 5580164 TEMPLATE 5580164 ROD CURVE 5.5/6.0 NA MEDTRONIC SOFAMOR DANEK, INC.
46 00763000140205 5580154 TEMPLATE 5580154 ROD CURVE 4.75 na MEDTRONIC SOFAMOR DANEK, INC.
47 00763000078980 EX0817017 RETRACTOR EX0817017 BIOPSY DRILL Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
48 00763000078959 EX0817014 DRILL EX0817014 BIOPSY CENTER Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
49 00763000078935 EX0817012 DRILL EX0817012 CENTER Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC.
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