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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 - 00843210139203

32mm x 24mm, 20°, 16mm Ti Spacer
Altus Spine, LLC
FA32242016T
In Commercial Distribution

  • 00843210139203 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139197

32mm x 24mm, 20°, 14mm Ti Spacer
Altus Spine, LLC
FA32242014T
In Commercial Distribution

  • 00843210139197 ()


  • Spinal implant trial

Brickyard ALIF - 00843210139180

32mm x 24mm, 20°, 12mm Ti Spacer
Altus Spine, LLC
FA32242012T
In Commercial Distribution

  • 00843210139180 ()


  • 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

Indy - 00843210138534

32mm x 24mm, 20°, 15mm Ti Spacer
Altus Spine, LLC
FA32242015T
In Commercial Distribution

  • 00843210138534 ()


  • Spinal implant trial

Indy - 00843210138527

32mm x 24mm, 20°, 13mm Ti Spacer
Altus Spine, LLC
FA32242013T
In Commercial Distribution

  • 00843210138527 ()


  • Spinal implant trial

Indy - 00843210138329

42mm x 30mm, 20°, 19mm PEEK Spacer
Altus Spine, LLC
FA42302019
In Commercial Distribution

  • 00843210138329 ()


  • Spinal implant trial

Indy - 00843210138312

42mm x 30mm, 20°, 17mm PEEK Spacer
Altus Spine, LLC
FA42302017
In Commercial Distribution

  • 00843210138312 ()


  • Spinal implant trial

Indy - 00843210138305

42mm x 30mm, 20°, 15mm PEEK Spacer
Altus Spine, LLC
FA42302015
In Commercial Distribution

  • 00843210138305 ()


  • Spinal implant trial
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