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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 - 00843210137902

34mm x 26mm, 20°, 19mm PEEK Spacer
Altus Spine, LLC
FA34262019
In Commercial Distribution

  • 00843210137902 ()


  • Spinal implant trial

Indy - 00843210137896

34mm x 26mm, 20°, 17mm PEEK Spacer
Altus Spine, LLC
FA34262017
In Commercial Distribution

  • 00843210137896 ()


  • Spinal implant trial

Indy - 00843210137889

34mm x 26mm, 20°, 15mm PEEK Spacer
Altus Spine, LLC
FA34262015
In Commercial Distribution

  • 00843210137889 ()


  • Spinal implant trial

Indy - 00843210137872

34mm x 26mm, 20°, 13mm PEEK Spacer
Altus Spine, LLC
FA34262013
In Commercial Distribution

  • 00843210137872 ()


  • Spinal implant trial

Indy - 00843210137674

32mm x 24mm, 20°, 19mm PEEK Spacer
Altus Spine, LLC
FA32242019
In Commercial Distribution

  • 00843210137674 ()


  • Spinal implant trial

Indy - 00843210137667

32mm x 24mm, 20°, 17mm PEEK Spacer
Altus Spine, LLC
FA32242017
In Commercial Distribution

  • 00843210137667 ()


  • Spinal implant trial

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
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