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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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NA - 00195377164032

XATP MIS Penfield Blade, 220mm C-C Right
Nuvasive, Inc.
Z200282-221
In Commercial Distribution

  • 00195377164032 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377164025

XATP MIS Penfield Blade, 220mm C-C Left
Nuvasive, Inc.
Z200282-220
In Commercial Distribution

  • 00195377164025 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377164018

XATP MIS Penfield Blade, 200mm C-C Right
Nuvasive, Inc.
Z200282-201
In Commercial Distribution

  • 00195377164018 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377164001

XATP MIS Penfield Blade, 200mm C-C Left
Nuvasive, Inc.
Z200282-200
In Commercial Distribution

  • 00195377164001 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377163998

XATP MIS Penfield Blade, 160mm C-C Right
Nuvasive, Inc.
Z200282-161
In Commercial Distribution

  • 00195377163998 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377163981

XATP MIS Penfield Blade, 160mm C-C Left
Nuvasive, Inc.
Z200282-160
In Commercial Distribution

  • 00195377163981 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377163974

XATP MIS Penfield Blade, 140mm C-C Right
Nuvasive, Inc.
Z200282-141
In Commercial Distribution

  • 00195377163974 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377163967

XATP MIS Penfield Blade, 140mm C-C Left
Nuvasive, Inc.
Z200282-140
In Commercial Distribution

  • 00195377163967 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377163950

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

  • 00195377163950 ()


  • Internal spinal fixation procedure kit, reusable

NA - 00195377163943

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

  • 00195377163943 ()


  • Internal spinal fixation procedure kit, reusable
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