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 Class Implantable

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ARM16S Bender, 6.35mm In-Situ Coronal L
Nuvasive, Inc.
7459133
In Commercial Distribution

  • 00887517485137 ()


  • Internal spinal fixation procedure kit, reusable
ARM16S Bender, 6.35mm In-Situ Sagittal R
Nuvasive, Inc.
7459132
In Commercial Distribution

  • 00887517485120 ()


  • Internal spinal fixation procedure kit, reusable
ARM16S Bender, 6.35mm In-Situ Sagittal L
Nuvasive, Inc.
7459131
In Commercial Distribution

  • 00887517485113 ()


  • Internal spinal fixation procedure kit, reusable
ARM16S Counter Torque
Nuvasive, Inc.
7459128
In Commercial Distribution

  • 00887517485083 ()


  • Internal spinal fixation procedure kit, reusable
Armada Counter Torque, Offset Conn Open
Nuvasive, Inc.
7459118
In Commercial Distribution

  • 00887517485007 ()


  • Internal spinal fixation procedure kit, reusable
Armada Ti Counter Torque, Closed Iliac
Nuvasive, Inc.
7459114
In Commercial Distribution

  • 00887517484970 ()


  • Internal spinal fixation procedure kit, reusable
Armada Counter Torque, 5.5mm Reduction
Nuvasive, Inc.
7459105
In Commercial Distribution

  • 00887517484932 ()


  • Internal spinal fixation procedure kit, reusable
Armada Ti Rod Cutter, In-situ
Nuvasive, Inc.
7459068
In Commercial Distribution

  • 00887517484857 ()


  • Internal spinal fixation procedure kit, reusable
Armada Curette Probe, Small with Stopper
Nuvasive, Inc.
7459067
In Commercial Distribution

  • 00887517484840 ()


  • Internal spinal fixation procedure kit, reusable
Armada Ti Rod Bender, Right
Nuvasive, Inc.
7459065
In Commercial Distribution

  • 00887517484826 ()


  • Internal spinal fixation procedure kit, reusable
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