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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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XATP MIS Penfield Blade, 80mm C-C Right
Nuvasive, Inc.
Z200282-081
In Commercial Distribution

  • 00195377165862 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 80mm C-C Left
Nuvasive, Inc.
Z200282-080
In Commercial Distribution

  • 00195377165855 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Right
Nuvasive, Inc.
Z200282-061
In Commercial Distribution

  • 00195377165848 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Left
Nuvasive, Inc.
Z200282-060
In Commercial Distribution

  • 00195377165831 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 80mm C-C Right
Nuvasive, Inc.
Z200282-81
In Commercial Distribution

  • 00195377164070 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 80mm C-C Left
Nuvasive, Inc.
Z200282-80
In Commercial Distribution

  • 00195377164063 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Right
Nuvasive, Inc.
Z200282-61
In Commercial Distribution

  • 00195377164056 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 60mm C-C Left
Nuvasive, Inc.
Z200282-60
In Commercial Distribution

  • 00195377164049 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 220mm C-C Right
Nuvasive, Inc.
Z200282-221
In Commercial Distribution

  • 00195377164032 ()


  • Internal spinal fixation procedure kit, reusable
XATP MIS Penfield Blade, 220mm C-C Left
Nuvasive, Inc.
Z200282-220
In Commercial Distribution

  • 00195377164025 ()


  • Internal spinal fixation procedure kit, reusable
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