NVISION BIOMEDICAL TECHNOLOGIES, INC.
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NVISION BIOMEDICAL TECHNOLOGIES, INC.
| NVISION BIOMEDICAL TECHNOLOGIES, INC. | ||||
| CATALOG # | QTY | PRICE | DESCRIPTION | |
| ACE-005-L | 0 | - | ||
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| ACE-012-L | 0 | - | ||
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| ACE-605-L | 0 | - | ||
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| ACE-606-L | 0 | - | ||
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| ACE-608-L | 0 | - | ||
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| ACE-611-L | 0 | - | ||
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| ACE-612-L | 0 | - | ||
| ACE-612-S | 0 | - | ||
| ACP-425-20V | 0 | - | ||
| ACP-475-14V | 0 | - | ||
| ACP-475-16V | 0 | - | ||
| ACP-475-18V | 0 | - | ||
| ACP-475-20V | 0 | - | ||
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| ALE-0616-L | 0 | - | ||
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| ALE-0618-L | 0 | - | ||
| ALE-0618-S | 0 | - | ||
| ALE-0620-L | 0 | - | ||
| ALE-0620-S | 0 | - | ||
| ALE-1210-S | 0 | - | ||
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tangis
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Anterior Cervical Plating System, 4.25mm dia. 20mm long variable screw. The Tangis Anterior Cervical Plate is intended for anterior screw fixation to the cervical spine. Itis to be used in skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to T1). The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with: • degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), • spondylolisthesis, • trauma (i.e. fractures or dislocations), • tumors, • deformity (defined as kyphosis, lordosis, or scoliosis), • pseudarthrosis, • failed previous fusion, • spinal stenosis
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tangis
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Anterior Cervical Plating System, 4.75mm dia. 20mm long variable screw
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tangis
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Anterior Cervical Plating System, 4.75mm dia. 18mm long variable screw
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tangis
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Anterior Cervical Plating System, 4.75mm dia. 16mm long variable screw
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tangis
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Anterior Cervical Plating System, 4.75mm dia. 14mm long variable screw. The Tangis Anterior Cervical Plate is intended for anterior screw fixation to the cervical spine. It is to be used in skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to T1). The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with: • degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), • spondylolisthesis, • trauma (i.e. fractures or dislocations), • tumors, • deformity (defined as kyphosis, lordosis, or scoliosis), • pseudarthrosis, • failed previous fusion, • spinal stenosis