NVISION BIOMEDICAL TECHNOLOGIES, INC.

Address:4590 Lockhill Selma,San Antonio,TX,78249,US

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- Catalog Number :

Device Description : TLIF Encoded 11x35 12mm 7 Degree

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : TLIF Encoded 11x35 13mm 7 Degree

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : TLIF Encoded 11x35 14mm 7 Degree

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : TLIF Encoded 11x35 15mm 7 Degree

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : PLIF Encoded 10x22 15mm 0 Degrees

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Buttress Plate 15mm long, 8 degree. The Boundary Anterior Lumbar Buttress Plate Buttress Plate 15mm long, 8 degree. The Boundary Anterior Lumbar Buttress Plate is intended to stabilize the allograft or autograft at one level (L1-S1) as an aid to spinal fusion and to provide temporary stabilization and augment development of a solid spinal fusion. It may be used alone or with other anterior, anterolateral, or posterior spinal systems made of compatible materials. This device is not intended for load bearing applications.

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : KWQ

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Buttress Plate 15mm long, 0 degree. The Boundary Anterior Lumbar Buttress Plate Buttress Plate 15mm long, 0 degree. The Boundary Anterior Lumbar Buttress Plate is intended to stabilize the allograft or autograft at one level (L1-S1) as an aid to spinal fusion and to provide temporary stabilization and augment development of a solid spinal fusion. It may be used alone or with other anterior, anterolateral, or posterior spinal systems made of compatible materials. This device is not intended for load bearing applications.

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : KWQ

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Buttress Plate 20mm long, 8 degree. The Boundary Anterior Lumbar Buttress Plate Buttress Plate 20mm long, 8 degree. The Boundary Anterior Lumbar Buttress Plate is intended to stabilize the allograft or autograft at one level (L1-S1) as an aid to spinal fusion and to provide temporary stabilization and augment development of a solid spinal fusion. It may be used alone or with other anterior, anterolateral, or posterior spinal systems made of compatible materials. This device is not intended for load bearing applications.

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : KWQ

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Buttress Plate 20mm long, 0 degree. The Boundary Anterior Lumbar Buttress Plate Buttress Plate 20mm long, 0 degree. The Boundary Anterior Lumbar Buttress Plate is intended to stabilize the allograft or autograft at one level (L1-S1) as an aid to spinal fusion and to provide temporary stabilization and augment development of a solid spinal fusion. It may be used alone or with other anterior, anterolateral, or posterior spinal systems made of compatible materials. This device is not intended for load bearing applications.

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : KWQ

Prescription Use : Yes

Device Count : 1

- Catalog Number :

Device Description : Buttress Plate 25mm long, 8 degree. The Boundary Anterior Lumbar Buttress Plate Buttress Plate 25mm long, 8 degree. The Boundary Anterior Lumbar Buttress Plate is intended to stabilize the allograft or autograft at one level (L1-S1) as an aid to spinal fusion and to provide temporary stabilization and augment development of a solid spinal fusion. It may be used alone or with other anterior, anterolateral, or posterior spinal systems made of compatible materials. This device is not intended for load bearing applications.

Device Class : 2

Duns Number: 047486041

Premarket Exempt : No

Product Code : KWQ

Prescription Use : Yes

Device Count : 1