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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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Indy - 00843210137650

32mm x 24mm, 20°, 15mm PEEK Spacer
Altus Spine, LLC
FA32242015
In Commercial Distribution

  • 00843210137650 ()


  • Spinal implant trial

Indy - 00843210137643

32mm x 24mm, 20°, 13mm PEEK Spacer
Altus Spine, LLC
FA32242013
In Commercial Distribution

  • 00843210137643 ()


  • Spinal implant trial

Brickyard ALIF - 00843210128795

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

  • 00843210128795 ()


  • Spinal implant trial

Brickyard ALIF - 00843210128788

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

  • 00843210128788 ()


  • Spinal implant trial

Brickyard ALIF - 00843210128771

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

  • 00843210128771 ()


  • Spinal implant trial

Brickyard ALIF - 00843210128764

38mm x 27mm, 20°, 14mm PEEK Spacer
Altus Spine, LLC
FA38272014
In Commercial Distribution

  • 00843210128764 ()


  • Spinal implant trial

Brickyard ALIF - 00843210127767

38mm x 27mm, 20°, 20mm Ti Spacer
Altus Spine, LLC
FA38272020T
In Commercial Distribution

  • 00843210127767 ()


  • Spinal implant trial

Brickyard ALIF - 00843210127750

38mm x 27mm, 20°, 18mm Ti Spacer
Altus Spine, LLC
FA38272018T
In Commercial Distribution

  • 00843210127750 ()


  • Spinal implant trial

Brickyard ALIF - 00843210127743

38mm x 27mm, 20°, 16mm Ti Spacer
Altus Spine, LLC
FA38272016T
In Commercial Distribution

  • 00843210127743 ()


  • Spinal implant trial

Brickyard ALIF - 00843210127736

38mm x 27mm, 20°, 14mm Ti Spacer
Altus Spine, LLC
FA38272014T
In Commercial Distribution

  • 00843210127736 ()


  • Spinal implant trial
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