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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
- 04047844112403 ()
- 13x10x20mm
TST00131020
- 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, angled
In Commercial Distribution
- 04047844112397 ()
- 12x10x20mm
TST06121020
- 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
- 04047844112380 ()
- 12x10x20mm
TST00121020
- 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
- 04047844112373 ()
- 10x10x20mm
TST00101020
- 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
- 04047844112366 ()
- 9x10x20mm
TST00091020
- 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
- 04047844112359 ()
- 8x10x20mm
TST00081020
- 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
- 04047844112342 ()
- 7x10x20mm
TST00071020
- 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
- 04047844112335 ()
- 6x10x20mm
TST00061020
- 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
- 04047844112328 ()
- 11x10x20mm
TST00111020
- 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, angled
In Commercial Distribution
- 04047844112519 ()
- 15x10x20mm
TST06151020
- 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, angled
In Commercial Distribution
- 04047844112502 ()
- 14x10x20mm
TST06141020
- 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, angled
In Commercial Distribution
- 04047844112496 ()
- 13x10x20mm
TST06131020
- 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, angled
In Commercial Distribution
- 04047844112489 ()
- 12x10x20mm
TST16121020
- 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, angled
In Commercial Distribution
- 04047844112311 ()
- 12x10x24mm
TST20121024
- Metallic spinal interbody fusion cage
The HistoCore SPECTRA ST is an in-vitro diagnostics instrument. The HistoCore SPECTRA ST is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens.
Leica Biosystems Nussloch GmbH
000000014051254354
In Commercial Distribution
- 04049188191953 ()
- Device Size Text, specify:
14051254354
- Microscope slide stainer IVD
Nitrile Powder Free Textured Black Exam Gloves, Non- Sterile, Chemo Tested, size XL
Uniseal
775-9
In Commercial Distribution
- 30744514077592 ()
- 20744514077595 ()
- 10744514077598 ()
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Nitrile Powder Free Textured Black Exam Gloves, Non- Sterile, Chemo Tested, size L
Uniseal
775-8
In Commercial Distribution
- 30744514077585 ()
- 20744514077588 ()
- 10744514077581 ()
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Nitrile Powder Free Textured Black Exam Gloves, Non- Sterile, Chemo Tested, size M
Uniseal
775-7
In Commercial Distribution
- 30744514077578 ()
- 20744514077571 ()
- 10744514077574 ()
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Nitrile Powder Free Textured Black Exam Gloves, Non- Sterile, Chemo Tested, size S
Uniseal
775-6
In Commercial Distribution
- 30744514077561 ()
- 20744514077564 ()
- 10744514077567 ()
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Nitrile Powder Free Textured Black Exam Gloves, Non- Sterile, Chemo Tested, size XXL
Uniseal
775-0
In Commercial Distribution
- 30744514077509 ()
- 20744514077502 ()
- 10744514077505 ()
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Symmetry® Retractor, St. Marks Deep Pelvic, w/Lip, 15° Angle, 11 in Working Length
SYMMETRY SURGICAL INC.
50-9028S
In Commercial Distribution
- 00887482074800 ()
- Length: 11 Inch
50-9028S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St Marks Deep Pelvic, 15° Angle, w/Lip, 9 in Working Length, 13 2/5 in, 34 cm
SYMMETRY SURGICAL INC.
50-9027S
In Commercial Distribution
- 00887482074794 ()
- Length: 13.4 Inch
50-9027S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks Deep Pelvic, w/o Lip
SYMMETRY SURGICAL INC.
50-9026S
In Commercial Distribution
- 00887482074787 ()
50-9026S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks Deep Pelvic, w/Lip, 15° Angle, 7 in Blade Length, 13 in, 330 mm
SYMMETRY SURGICAL INC.
50-9025S
In Commercial Distribution
- 00887482074770 ()
- Length: 13 Inch
50-9025S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks, w/Lip, 5 in Working Length, 11 1/2 in
SYMMETRY SURGICAL INC.
50-9024S
In Commercial Distribution
- 00887482074763 ()
- Length: 11.5 Inch
50-9024S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks Deep Pelvic, w/Lip
SYMMETRY SURGICAL INC.
50-9023S
In Commercial Distribution
- 00887482074749 ()
50-9023S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks Deep Pelvic, w/Lip
SYMMETRY SURGICAL INC.
50-9020S
In Commercial Distribution
- 00887482074725 ()
50-9020S
- Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks, w/Lip, 2-2 1/2 in Taper, 7 in
SYMMETRY SURGICAL INC.
502-002
In Commercial Distribution
- 00887482074466 ()
- Length: 7 Inch
502-002
- Hand-held surgical retractor, reusable
Linear ST, 70cm 8 Contact Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-70
In Commercial Distribution
- M365SC2218700 ()
- 70 cm Length
SC-2218-70
- Analgesic spinal cord electrical stimulation system
Linear ST, 50cm 8 Contact Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-50
In Commercial Distribution
- M365SC2218500 ()
- 50 cm Length
SC-2218-50
- Analgesic spinal cord electrical stimulation system