SEARCH RESULTS FOR: (*Make St. Paul*)(7518 results)

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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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2.0MM TI CANN SCREW + ST - 18MM
Tyber Medical, LLC
04.353.018S
In Commercial Distribution

  • 00810080883574 ()
04.353.018S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 17MM
Tyber Medical, LLC
04.353.017S
In Commercial Distribution

  • 00810080883567 ()
04.353.017S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 16MM
Tyber Medical, LLC
04.353.016S
In Commercial Distribution

  • 00810080883550 ()
04.353.016S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 15MM
Tyber Medical, LLC
04.353.015S
In Commercial Distribution

  • 00810080883543 ()
04.353.015S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 14MM
Tyber Medical, LLC
04.353.014S
In Commercial Distribution

  • 00810080883536 ()
04.353.014S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 13MM
Tyber Medical, LLC
04.353.013S
In Commercial Distribution

  • 00810080883529 ()
04.353.013S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 12MM
Tyber Medical, LLC
04.353.012S
In Commercial Distribution

  • 00810080883512 ()
04.353.012S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 11MM
Tyber Medical, LLC
04.353.011S
In Commercial Distribution

  • 00810080883505 ()
04.353.011S

  • Orthopaedic bone screw (non-sliding)
2.0MM TI CANN SCREW + ST - 10MM
Tyber Medical, LLC
04.353.010S
In Commercial Distribution

  • 00810080883499 ()
04.353.010S

  • Orthopaedic bone screw (non-sliding)
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
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