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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 - 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

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

Indy - 00843210138107

38mm x 27mm, 20°, 15mm PEEK Spacer
Altus Spine, LLC
FA38272015
In Commercial Distribution

  • 00843210138107 ()


  • Spinal implant trial

Indy - 00843210138091

38mm x 27mm, 20°, 13mm PEEK Spacer
Altus Spine, LLC
FA38272013
In Commercial Distribution

  • 00843210138091 ()


  • Spinal implant trial

Indy - 00843210137902

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

  • 00843210137902 ()


  • Spinal implant trial
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