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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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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

  • 04047844114759 ()

  • 14x9x20mm
TRT20140920

  • 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

  • 04047844114742 ()

  • 13x9x20mm
TRT20130920

  • 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

  • 04047844114735 ()

  • 12x9x20mm
TRT20120920

  • 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

  • 04047844114711 ()

  • 17x9x20mm
TRT20170920

  • Metallic spinal interbody fusion cage
No Description
Baylis Medical Technologies Inc
PSZ-400-305
Not in Commercial Distribution



  • Suturing unit, single-use
No Description
BIOPRO, INC.
10724
In Commercial Distribution

  • M209107240 ()


  • Orthopaedic bone screw, non-bioabsorbable, sterile
Pressure Injectable Three-Lumen PICC Kit pre-loaded with Arrow(R) VPS TipTracker(TM) Stylet
TELEFLEX INCORPORATED
IPN056674
In Commercial Distribution

  • 20801902167648 ()
  • 10801902167641 ()
ASK-35563-MHBS

  • Peripherally-inserted central venous catheter
Pressure Injectable Two-Lumen PICC Kit pre-loaded with Arrow(R) VPS TipTracker(TM) Stylet
TELEFLEX INCORPORATED
IPN056673
In Commercial Distribution

  • 20801902167631 ()
  • 10801902167634 ()
ASK-35552-MHBS

  • Peripherally-inserted central venous catheter
Pressure Injectable One-Lumen PICC Kit pre-loaded with Arrow(R) VPS TipTracker(TM) Stylet
TELEFLEX INCORPORATED
IPN056672
In Commercial Distribution

  • 20801902167624 ()
  • 10801902167627 ()
ASK-35541-MHBS

  • Peripherally-inserted central venous catheter
PSI Kit for use with 7 - 7.5 Fr. Catheters
TELEFLEX INCORPORATED
IPN916309
In Commercial Distribution

  • 20801902164272 ()
  • 10801902164275 ()
PH-09806

  • Vascular catheter introduction set, nonimplantable
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