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

Show Filters

RELINE-O Trial, 8mm H Lamina Ang W L-pop
Nuvasive, Inc.
1200028
In Commercial Distribution

  • 00195377047113 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial, 7mm H Lamina Ang W L-pop
Nuvasive, Inc.
1200027
In Commercial Distribution

  • 00195377047106 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial, 6mm H Lamina Ang W L-pop
Nuvasive, Inc.
1200026
In Commercial Distribution

  • 00195377047090 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial, 5mm H Lamina Ang W L-pop
Nuvasive, Inc.
1200025
In Commercial Distribution

  • 00195377047083 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial,12mm H Lamina Ang N L-pop
Nuvasive, Inc.
1200024
In Commercial Distribution

  • 00195377047076 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial,11mm H Lamina Ang N L-pop
Nuvasive, Inc.
1200023
In Commercial Distribution

  • 00195377047069 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial,10mm H Lamina Ang N L-pop
Nuvasive, Inc.
1200022
In Commercial Distribution

  • 00195377047052 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial, 9mm H Lamina Ang N L-pop
Nuvasive, Inc.
1200021
In Commercial Distribution

  • 00195377047045 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial, 8mm H Lamina Ang N L-pop
Nuvasive, Inc.
1200020
In Commercial Distribution

  • 00195377047038 ()


  • Internal spinal fixation procedure kit, reusable
RELINE-O Trial, 7mm H Lamina Ang N L-pop
Nuvasive, Inc.
1200019
In Commercial Distribution

  • 00195377047021 ()


  • Internal spinal fixation procedure kit, reusable
< 1 ... 122 123 124 125 126 ... 485 >