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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 - 00843210142418

38mm x 27mm, 20°, 15mm Ti Spacer
Altus Spine, LLC
FA38272015T
In Commercial Distribution

  • 00843210142418 ()


  • 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 - 00843210139487

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

  • 00843210139487 ()


  • 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 - 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

Indy - 00843210138121

38mm x 27mm, 20°, 19mm PEEK Spacer
Altus Spine, LLC
FA38272019
In Commercial Distribution

  • 00843210138121 ()


  • Spinal implant trial

Indy - 00843210138114

38mm x 27mm, 20°, 17mm PEEK Spacer
Altus Spine, LLC
FA38272017
In Commercial Distribution

  • 00843210138114 ()


  • Spinal implant trial
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