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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XATP MIS Penfield Blade, 100mm C-C Right
Nuvasive, Inc.
Z200282-101
In Commercial Distribution

  • 00195377163950 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 100mm C-C Left
Nuvasive, Inc.
Z200282-100
In Commercial Distribution

  • 00195377163943 ()


  • Internal spinal fixation procedure kit, reusable
XLIF Paddle Sizer, 12x18mm Angled
Nuvasive, Inc.
Z200123-12
In Commercial Distribution

  • 00195377163936 ()


  • Internal spinal fixation procedure kit, reusable
XLIF Paddle Sizer, 10x18mm Angled
Nuvasive, Inc.
Z200123-10
In Commercial Distribution

  • 00195377163929 ()


  • Internal spinal fixation procedure kit, reusable
XLIF Paddle Sizer, 8x18mm Angled
Nuvasive, Inc.
Z200123-08
In Commercial Distribution

  • 00195377163912 ()


  • Internal spinal fixation procedure kit, reusable
XLIF Paddle Sizer, 4x18mm Angled
Nuvasive, Inc.
Z200123-04
In Commercial Distribution

  • 00195377163905 ()


  • Internal spinal fixation procedure kit, reusable
StruXure Retractor,22mm Lighted Long 2.0
Nuvasive, Inc.
Z118084-322
In Commercial Distribution

  • 00195377163899 ()


  • Internal spinal fixation procedure kit, reusable
StruXure Retractor,20mm Lighted Long 2.0
Nuvasive, Inc.
Z118084-320
In Commercial Distribution

  • 00195377163882 ()


  • Internal spinal fixation procedure kit, reusable
StruXure Retractor,18mm Lighted Long 2.0
Nuvasive, Inc.
Z118084-318
In Commercial Distribution

  • 00195377163875 ()


  • Internal spinal fixation procedure kit, reusable
XLIF Rasp, Single Sided Angled Down
Nuvasive, Inc.
Z116019-2
In Commercial Distribution

  • 00195377163868 ()


  • Internal spinal fixation procedure kit, reusable
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