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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 Class Implantable

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MaXcess-C Blade, 19x30mm Serrated Micro
Nuvasive, Inc.
Z700006-30
In Commercial Distribution

  • 00195377166203 ()


  • Internal spinal fixation procedure kit, reusable
Reline T-Handle, Distractor Dual Hinged
Nuvasive, Inc.
Z600472-300
In Commercial Distribution

  • 00195377166197 ()


  • Internal spinal fixation procedure kit, reusable
Reline Distractor Tip, Dual Hinged Left
Nuvasive, Inc.
Z600472-20
In Commercial Distribution

  • 00195377166173 ()


  • Internal spinal fixation procedure kit, reusable
Reline Distractor Tip,Dual Hinged ShortR
Nuvasive, Inc.
Z600472-11
In Commercial Distribution

  • 00195377166166 ()


  • Internal spinal fixation procedure kit, reusable
Reline Distractor Tip,Dual Hinged ShortL
Nuvasive, Inc.
Z600472-10
In Commercial Distribution

  • 00195377166159 ()


  • Internal spinal fixation procedure kit, reusable
Reline MAS Tap, Cannulated Detent,12.0mm
Nuvasive, Inc.
Z600471-120
In Commercial Distribution

  • 00195377166128 ()


  • Internal spinal fixation procedure kit, reusable
Reline MAS Tap, Cannulated Detent,11.5mm
Nuvasive, Inc.
Z600471-115
In Commercial Distribution

  • 00195377166111 ()


  • Internal spinal fixation procedure kit, reusable
Reline MAS Tap, Cannulated Detent,11.0mm
Nuvasive, Inc.
Z600471-110
In Commercial Distribution

  • 00195377166104 ()


  • Internal spinal fixation procedure kit, reusable
Reline MAS Tap, Cannulated Detent,10.0mm
Nuvasive, Inc.
Z600471-100
In Commercial Distribution

  • 00195377166081 ()


  • Internal spinal fixation procedure kit, reusable
Reline MAS Tap, Cannulated Detent, 9.5mm
Nuvasive, Inc.
Z600471-095
In Commercial Distribution

  • 00195377166074 ()


  • Internal spinal fixation procedure kit, reusable
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