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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Mi1210 SYNCHRONY ST +MEDIUM - 09008737331832

Cochlear Implant
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
33183
In Commercial Distribution

  • 09008737331832 ()
33334

  • Cochlear implant system electrode array assembly

Mi1210 SYNCHRONY ST +STANDARD - 09008737331825

Cochlear Implant
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
33182
In Commercial Distribution

  • 09008737331825 ()
33333

  • Cochlear implant system electrode array assembly

Mi1210 SYNCHRONY ST +FLEX26 - 09008737366193

Cochlear Implant
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
36619
In Commercial Distribution

  • 09008737366193 ()
36631

  • Cochlear implant system electrode array assembly

Magic Multi Abutment ST - 08800039371650

No Description
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
MTCN45
In Commercial Distribution

  • 08800039371650 ()


  • Dental implant system

Magic Multi Abutment ST - 08800039371643

No Description
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
MTCN55
In Commercial Distribution

  • 08800039371643 ()


  • Dental implant system

TETRIS R ST 20° - 04047844116258

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

  • 04047844116258 ()

  • 18x9x32mm
TRT20180932

  • Metallic spinal interbody fusion cage

TETRIS R ST 20° - 04047844116241

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

  • 04047844116241 ()

  • 17x9x32mm
TRT20170932

  • Metallic spinal interbody fusion cage

TETRIS R ST 20° - 04047844116234

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

  • 04047844116234 ()

  • 16x9x32mm
TRT20160932

  • Metallic spinal interbody fusion cage

TETRIS R ST 16° - 04047844116173

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

  • 04047844116173 ()

  • 18x9x32mm
TRT16180932

  • Metallic spinal interbody fusion cage

TETRIS R ST 16° - 04047844116166

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

  • 04047844116166 ()

  • 17x9x32mm
TRT16170932

  • Metallic spinal interbody fusion cage
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