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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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42mm x 30mm, 8°, 16mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA42300816
In Commercial Distribution

  • 00843210128887 ()


  • Spinal implant trial
42mm x 30mm, 8°, 14mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA42300814
In Commercial Distribution

  • 00843210128870 ()


  • Spinal implant trial
42mm x 30mm, 8°, 12mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA42300812
In Commercial Distribution

  • 00843210128863 ()


  • Spinal implant trial
42mm x 30mm, 8°, 10mm PEEK Spacer - Brickyard ALIF System
Altus Spine, LLC
FA42300810
In Commercial Distribution

  • 00843210128856 ()


  • Spinal implant trial
38mm x 27mm, 25°, 20mm PEEK Spacer
Altus Spine, LLC
FA38272520
In Commercial Distribution

  • 00843210128832 ()


  • Spinal implant trial
38mm x 27mm, 25°, 18mm PEEK Spacer
Altus Spine, LLC
FA38272518
In Commercial Distribution

  • 00843210128825 ()


  • Spinal implant trial
38mm x 27mm, 25°, 16mm PEEK Spacer
Altus Spine, LLC
FA38272516
In Commercial Distribution

  • 00843210128818 ()


  • Spinal implant trial
38mm x 27mm, 20°, 20mm PEEK Spacer
Altus Spine, LLC
FA38272020
In Commercial Distribution

  • 00843210128795 ()


  • Spinal implant trial
38mm x 27mm, 20°, 18mm PEEK Spacer
Altus Spine, LLC
FA38272018
In Commercial Distribution

  • 00843210128788 ()


  • Spinal implant trial
38mm x 27mm, 20°, 16mm PEEK Spacer
Altus Spine, LLC
FA38272016
In Commercial Distribution

  • 00843210128771 ()


  • Spinal implant trial
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