Spinal Vertebral Body Replacement Device Suppliers
Limit companies to: Worldwide USA
Synthes Gmbh | Address: Eimattstrasse 3, Oberdorf CH-4436, Switzerland
www.synthes.com | Send Inquiry | Phone: +41-(61)-9656666
FDA Registration: 8030965
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Laser Power Probe, Laparoscopic Probes, Guiding Probes, Flexible Depth Gauge (FDA Code: HTJ), ...
Synthes GmbH develops, produces and markets instruments, implants & biomaterials for the surgical fixation, correction & regeneration of the skeleton & its soft tissues. Trauma implants and instrument more...
www.synthes.com | Send Inquiry | Phone: +41-(61)-9656666
FDA Registration: 8030965
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Laser Power Probe, Laparoscopic Probes, Guiding Probes, Flexible Depth Gauge (FDA Code: HTJ), ...
Synthes GmbH develops, produces and markets instruments, implants & biomaterials for the surgical fixation, correction & regeneration of the skeleton & its soft tissues. Trauma implants and instrument more...
Co-Ligne Ag | Address: Utoquai 43, Zurich CH-8008, Switzerland
www.coligne.com | Send Inquiry | Phone: +41-(43)-343 8000
Products: Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), ...
Co-Ligne Ag specializes in cylindrical fiber reinforced implants. Our proprietary technology built ostaPek carbon compositive VBR system,is an implant system that provides better stability for correct more...
www.coligne.com | Send Inquiry | Phone: +41-(43)-343 8000
Products: Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), ...
Co-Ligne Ag specializes in cylindrical fiber reinforced implants. Our proprietary technology built ostaPek carbon compositive VBR system,is an implant system that provides better stability for correct more...
Sintea Biotech Spa | Address: Via Aquileia 33/h, Baranzate 20021, Italy
Phone: +39-(2)-38204222
FDA Registration: 3003475199
Products: Invasive Traction Component (FDA Code: JEC), Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), ...
Sintea Biotech Spa deals with anterior cervical plating systems, screws, traction components and trauma fixation systems. more...
Phone: +39-(2)-38204222
FDA Registration: 3003475199
Products: Invasive Traction Component (FDA Code: JEC), Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), ...
Sintea Biotech Spa deals with anterior cervical plating systems, screws, traction components and trauma fixation systems. more...
Signus Medizintechnik GmbH | Address: Rannenbergring 54, Alzenau 63755, Germany 
FDA Registration: 9615021
Products: Cosmetic Microsurgical Instruments, Titanium Microsurgical Instruments, Microsurgical Instruments (FDA Code: GZX), Cardiovascular Surgical Instrument (FDA Code: DWS), General Surgical Manual Instrument (FDA Code: MDM), Manual Surgical Instrument, ...
Signus Medizintechnik GmbH offers microsurgical instruments and manual surgical instruments. more...
FDA Registration: 9615021
Products: Cosmetic Microsurgical Instruments, Titanium Microsurgical Instruments, Microsurgical Instruments (FDA Code: GZX), Cardiovascular Surgical Instrument (FDA Code: DWS), General Surgical Manual Instrument (FDA Code: MDM), Manual Surgical Instrument, ...
Signus Medizintechnik GmbH offers microsurgical instruments and manual surgical instruments. more...
Stryker Trauma Gmbh | Address: Prof.-Kuentscher-Strasse 1-5, Schoenkirchen D-24232, Germany
Phone: +49-(4348)-702-0
FDA Registration: 9610622 Year Established: 1941
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Flexible Depth Gauge (FDA Code: HTJ), Invasive Traction Component (FDA Code: JEC), Orthopedic Manual Surgical Instrument (FDA Code: LXH), Pneumatic Powered Orthopedic Surgical Instrument & Accessory (FDA Code: HSZ), ...
Stryker Trauma GmbH offers orthopedic manual surgical instruments, pneumatic orthopedic power tool systems, screws and staples. more...
Phone: +49-(4348)-702-0
FDA Registration: 9610622 Year Established: 1941
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Flexible Depth Gauge (FDA Code: HTJ), Invasive Traction Component (FDA Code: JEC), Orthopedic Manual Surgical Instrument (FDA Code: LXH), Pneumatic Powered Orthopedic Surgical Instrument & Accessory (FDA Code: HSZ), ...
Stryker Trauma GmbH offers orthopedic manual surgical instruments, pneumatic orthopedic power tool systems, screws and staples. more...
Aesculap Ag | Address: 1120, Tuttlingen, Donau D-78532, Germany
www.aesculap.de | Send Inquiry | Phone: +94-(610)-9849074
FDA Registration: 9610612
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Laser Power Probe, Laparoscopic Probes, Guiding Probes, Flexible Depth Gauge (FDA Code: HTJ), ...
Aesculap Ag offers instruments for minimal invasive surgery. Our product range includes surgical instruments for open or minimally invasive approaches, implants for orthopedic, neuro and spinal surger more...
www.aesculap.de | Send Inquiry | Phone: +94-(610)-9849074
FDA Registration: 9610612
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Laser Power Probe, Laparoscopic Probes, Guiding Probes, Flexible Depth Gauge (FDA Code: HTJ), ...
Aesculap Ag offers instruments for minimal invasive surgery. Our product range includes surgical instruments for open or minimally invasive approaches, implants for orthopedic, neuro and spinal surger more...
Biedermann Motech GmbH & Co. KG | Address: 23, Bertha-von-Suttner-Street, Villingen-Schwenningen 78054, Germany
www.biedermann.com | Send Inquiry | Phone: +49-(7720)-85100
FDA Registration: 8010944
Products: Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), Metal Mesh (FDA Code: EZX), ...
Biedermann Motech GmbH & Co. KG specializec in the design and development of orthopedic implants and instruments used in spinal & trauma surgeries. We provide external & internal fixtures and plate & more...
www.biedermann.com | Send Inquiry | Phone: +49-(7720)-85100
FDA Registration: 8010944
Products: Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), Metal Mesh (FDA Code: EZX), ...
Biedermann Motech GmbH & Co. KG specializec in the design and development of orthopedic implants and instruments used in spinal & trauma surgeries. We provide external & internal fixtures and plate & more...
Creaspine | Address: Ptib Hopital Xavier Arnozan, Avenue Du Haut Leveque, Pessac 33600, France
www.creaspine.com | Phone: +33-(557)-102858
Products: Vertebral Body Distractor, Vertebral Body Replacement System, Bone Graft Impactor, Spinal Vertebral Body Replacement Device (FDA Code: MQP), ...
Creaspine deals with thoracolumbar vertebral body replacement system. Our thoracolumbar vertebral body replacement system comprises of Supstance® small and Supstance® large. Our thoracolumbar more...
www.creaspine.com | Phone: +33-(557)-102858
Products: Vertebral Body Distractor, Vertebral Body Replacement System, Bone Graft Impactor, Spinal Vertebral Body Replacement Device (FDA Code: MQP), ...
Creaspine deals with thoracolumbar vertebral body replacement system. Our thoracolumbar vertebral body replacement system comprises of Supstance® small and Supstance® large. Our thoracolumbar more...
LDR Medical | Address: Technopole De L'Aube, Bp2-10902, Cedex 9, Troyes, France
www.ldrmedical.com | Phone: +33-(03)-25823263
FDA Registration: 3004788213
Products: Calcium Compound Bone Void Filler (FDA Code: MQV), Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB), ...
LDR Medical provides products for both fusion and non-fusion surgery. Our products include Mobi™ artificial disc system, Roi® peek implementation system and Easyspine® pedicle screw syst more...
www.ldrmedical.com | Phone: +33-(03)-25823263
FDA Registration: 3004788213
Products: Calcium Compound Bone Void Filler (FDA Code: MQV), Spinal Interlaminal Fixation Appliance (FDA Code: KWP), Spinal Pedicle Fixation Orthosis (FDA Code: MNI), Spinal Vertebral Body Replacement Device (FDA Code: MQP), Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH), Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB), ...
LDR Medical provides products for both fusion and non-fusion surgery. Our products include Mobi™ artificial disc system, Roi® peek implementation system and Easyspine® pedicle screw syst more...
FDA Code / Regulation: MQP / 888.3060
A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.
Classification. Class II.
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