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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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Brickyard ALIF - 00843210140148

32mm x 24mm, 20°, 12mm PEEK Spacer
Altus Spine, LLC
FA32242012
In Commercial Distribution

  • 00843210140148 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139937

42mm x 30mm, 20°, 20mm Ti Spacer
Altus Spine, LLC
FA42302020T
In Commercial Distribution

  • 00843210139937 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139920

42mm x 30mm, 20°, 18mm Ti Spacer
Altus Spine, LLC
FA42302018T
In Commercial Distribution

  • 00843210139920 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139913

42mm x 30mm, 20°, 16mm Ti Spacer
Altus Spine, LLC
FA42302016T
In Commercial Distribution

  • 00843210139913 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139487

34mm x 26mm, 20°, 20mm Ti Spacer
Altus Spine, LLC
FA34262020T
In Commercial Distribution

  • 00843210139487 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139470

34mm x 26mm, 20°, 18mm Ti Spacer
Altus Spine, LLC
FA34262018T
In Commercial Distribution

  • 00843210139470 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139463

34mm x 26mm, 20°, 16mm Ti Spacer
Altus Spine, LLC
FA34262016T
In Commercial Distribution

  • 00843210139463 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139456

34mm x 26mm, 20°, 14mm Ti Spacer
Altus Spine, LLC
FA34262014T
In Commercial Distribution

  • 00843210139456 ()


  • Spinal implant trial

Indy - 00843210138558

32mm x 24mm, 20°, 19mm Ti Spacer
Altus Spine, LLC
FA32242019T
In Commercial Distribution

  • 00843210138558 ()


  • Spinal implant trial

Indy - 00843210138541

32mm x 24mm, 20°, 17mm Ti Spacer
Altus Spine, LLC
FA32242017T
In Commercial Distribution

  • 00843210138541 ()


  • Spinal implant trial
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