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The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, straight
In Commercial Distribution
- 04047844114346 ()
- 7x9x20mm
TRT00070920
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, straight
In Commercial Distribution
- 04047844114339 ()
- 6x9x20mm
TRT00060920
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, straight
In Commercial Distribution
- 04047844114322 ()
- 8x9x20mm
TRT00080920
- Metallic spinal interbody fusion cage
Lead Kit
ST. JUDE MEDICAL, INC.
3189
In Commercial Distribution
- 05415067047922 ()
- Length: 90.0000 Centimeter
3189
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
Femoral Venous Cannula
Edwards Lifesciences LLC
FTV024
In Commercial Distribution
- 00690103180138 ()
- 24 Fr. (8.0 mm) x 68 cm (26.8")
FTV024
- Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
- Cardiopulmonary bypass cannula, femoral
Femoral Venous Cannula
Edwards Lifesciences LLC
FTV020
In Commercial Distribution
- 00690103180121 ()
- 20 Fr. (6.7 mm) x 55 cm (21.6")
FTV020
- Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
- Cardiopulmonary bypass cannula, femoral
FEM-FLEX II Femoral Arterial Cannula
Edwards Lifesciences LLC
FEMII020AS
In Commercial Distribution
- 00690103168365 ()
- 20 Fr. (6.7 mm) x 15 cm (6")
FEMII020AS
- Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
- Cardiopulmonary bypass cannula, femoral
FEM-FLEX II Femoral Arterial Cannula
Edwards Lifesciences LLC
FEMII018AS
In Commercial Distribution
- 00690103168358 ()
- 18 Fr. (6.0 mm) x 15 cm (6")
FEMII018AS
- Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
- Cardiopulmonary bypass cannula, femoral
FEM-FLEX II Femoral Arterial Cannula
Edwards Lifesciences LLC
FEMII016AS
In Commercial Distribution
- 00690103168341 ()
- 16 Fr. (5.3 mm) x 15 cm (6")
FEMII016AS
- Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
- Cardiopulmonary bypass cannula, femoral
Femoral Venous Cannula
Edwards Lifesciences LLC
VFEM028
In Commercial Distribution
- 00690103146684 ()
- 28 Fr. (9.3 mm) x 68 cm (26.8")
VFEM028
- Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage
- Cardiopulmonary bypass cannula, femoral