SEARCH RESULTS FOR: (*purchase New Brunswick driver*)(15741 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 - 00843210142166

34mm x 26mm, 16°, 17mm Ti Spacer
Altus Spine, LLC
FA34261617T
In Commercial Distribution

  • 00843210142166 ()


  • Spinal implant trial

Indy - 00843210142159

34mm x 26mm, 16°, 15mm Ti Spacer
Altus Spine, LLC
FA34261615T
In Commercial Distribution

  • 00843210142159 ()


  • Spinal implant trial

Indy - 00843210142142

34mm x 26mm, 16°, 13mm Ti Spacer
Altus Spine, LLC
FA34261613T
In Commercial Distribution

  • 00843210142142 ()


  • Spinal implant trial

Indy - 00843210142135

34mm x 26mm, 16°, 11mm Ti Spacer
Altus Spine, LLC
FA34261611T
In Commercial Distribution

  • 00843210142135 ()


  • Spinal implant trial

Indy - 00843210142128

34mm x 26mm, 12°, 19mm Ti Spacer
Altus Spine, LLC
FA34261219T
In Commercial Distribution

  • 00843210142128 ()


  • Spinal implant trial

Brickyard ALIF - 00843210140919

42mm x 30mm, 25°, 20mm PEEK Spacer
Altus Spine, LLC
FA42302520
In Commercial Distribution

  • 00843210140919 ()


  • Spinal implant trial

Brickyard ALIF - 00843210140902

42mm x 30mm, 25°, 18mm PEEK Spacer
Altus Spine, LLC
FA42302518
In Commercial Distribution

  • 00843210140902 ()


  • Spinal implant trial

Brickyard ALIF - 00843210140896

42mm x 30mm, 20°, 20mm PEEK Spacer
Altus Spine, LLC
FA42302020
In Commercial Distribution

  • 00843210140896 ()


  • Spinal implant trial

Brickyard ALIF - 00843210140889

42mm x 30mm, 20°, 18mm PEEK Spacer
Altus Spine, LLC
FA42302018
In Commercial Distribution

  • 00843210140889 ()


  • Spinal implant trial

Brickyard ALIF - 00843210140872

42mm x 30mm, 20°, 16mm PEEK Spacer
Altus Spine, LLC
FA42302016
In Commercial Distribution

  • 00843210140872 ()


  • Spinal implant trial
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