SEARCH RESULTS FOR: (*One Satoshitg:(@hkotccc)tFIg*)(19878 results)

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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 - 00843210138435

32mm x 24mm, 12°, 13mm Ti Spacer
Altus Spine, LLC
FA32241213T
In Commercial Distribution

  • 00843210138435 ()


  • Spinal implant trial

Indy - 00843210138428

32mm x 24mm, 12°, 11mm Ti Spacer
Altus Spine, LLC
FA32241211T
In Commercial Distribution

  • 00843210138428 ()


  • Spinal implant trial

Indy - 00843210138411

32mm x 24mm, 12°, 9mm Ti Spacer
Altus Spine, LLC
FA32241209T
In Commercial Distribution

  • 00843210138411 ()


  • Spinal implant trial

Indy - 00843210138404

32mm x 24mm, 8°, 19mm Ti Spacer
Altus Spine, LLC
FA32240819T
In Commercial Distribution

  • 00843210138404 ()


  • Spinal implant trial

Indy - 00843210138398

32mm x 24mm, 8°, 17mm Ti Spacer
Altus Spine, LLC
FA32240817T
In Commercial Distribution

  • 00843210138398 ()


  • Spinal implant trial

Indy - 00843210138381

32mm x 24mm, 8°, 15mm Ti Spacer
Altus Spine, LLC
FA32240815T
In Commercial Distribution

  • 00843210138381 ()


  • Spinal implant trial

Indy - 00843210138374

32mm x 24mm, 8°, 13mm Ti Spacer
Altus Spine, LLC
FA32240813T
In Commercial Distribution

  • 00843210138374 ()


  • Spinal implant trial

Indy - 00843210138367

32mm x 24mm, 8°, 11mm Ti Spacer
Altus Spine, LLC
FA32240811T
In Commercial Distribution

  • 00843210138367 ()


  • Spinal implant trial

Indy - 00843210138350

32mm x 24mm, 8°, 9mm Ti Spacer
Altus Spine, LLC
FA32240809T
In Commercial Distribution

  • 00843210138350 ()


  • Spinal implant trial

Indy - 00843210138343

42mm x 30mm, 25°, 19mm PEEK Spacer
Altus Spine, LLC
FA42302519
In Commercial Distribution

  • 00843210138343 ()


  • Spinal implant trial
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