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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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Pre-Bent Spinal Rod
UNIFIED SPINE, LLC
508180
In Commercial Distribution

  • M9935081801 ()

  • 5.5mm x 30mm Pre-Bent Spinal Rod


  • Bone-screw internal spinal fixation system rod
Pre-Bent Spinal Rod
UNIFIED SPINE, LLC
508180
In Commercial Distribution

  • M9935081800 ()

  • 5.5mm x 30mm Pre-Bent Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508110
In Commercial Distribution

  • M9935081101 ()

  • 5.5mm x 300mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508110
In Commercial Distribution

  • M9935081100 ()

  • 5.5mm x 300mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508106
In Commercial Distribution

  • M9935081061 ()

  • 5.5mm x 200mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508106
In Commercial Distribution

  • M9935081060 ()

  • 5.5mm x 100mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508104
In Commercial Distribution

  • M9935081041 ()

  • 5.5mm x 100mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508104
In Commercial Distribution

  • M9935081040 ()

  • 5.5mm x 100mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508102
In Commercial Distribution

  • M9935081021 ()

  • 5.5mm x 50mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
Spinal Rod
UNIFIED SPINE, LLC
508102
In Commercial Distribution

  • M9935081020 ()

  • 5.5mm x 50mm Spinal Rod


  • Bone-screw internal spinal fixation system rod
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