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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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Reline Cervical Core Instrument 1 - Beta
Nuvasive, Inc.
BETRELCCOREINS1
In Commercial Distribution

  • 00195377043955 ()


  • Device sterilization/disinfection container, reusable
Reline Cervical Core Implant - Beta
Nuvasive, Inc.
BETRELCCOREIMP
In Commercial Distribution

  • 00195377043948 ()


  • Device sterilization/disinfection container, reusable
Excavation Navigation.S General Ins 2
Nuvasive, Inc.
EXGENNAVSINS2
In Commercial Distribution

  • 00195377043931 ()


  • Device sterilization/disinfection container, reusable
Excavation Navigation.S General Ins 1
Nuvasive, Inc.
EXGENNAVSINS1
In Commercial Distribution

  • 00195377043924 ()


  • Device sterilization/disinfection container, reusable
ACP Drill Guide, Variable Double Barrel
Nuvasive, Inc.
7786750
In Commercial Distribution

  • 00195377043764 ()


  • Internal spinal fixation procedure kit, reusable
ACP 1.9H Plate, 15mm 1-Level
Nuvasive, Inc.
18009115
In Commercial Distribution

  • 00195377043757 ()


  • Spinal fixation plate, non-bioabsorbable
ACP 1.9H Plate, 14mm 1-Level
Nuvasive, Inc.
18009114
In Commercial Distribution

  • 00195377043740 ()


  • Spinal fixation plate, non-bioabsorbable
ACP 1.6V Plate, 15mm 1-Level
Nuvasive, Inc.
18006115
In Commercial Distribution

  • 00195377043733 ()


  • Spinal fixation plate, non-bioabsorbable
ACP 1.6V Plate, 14mm 1-Level
Nuvasive, Inc.
18006114
In Commercial Distribution

  • 00195377043726 ()


  • Spinal fixation plate, non-bioabsorbable
ACP 2.1H Plate, 15mm 1-Level
Nuvasive, Inc.
18002115
In Commercial Distribution

  • 00195377043719 ()


  • Spinal fixation plate, non-bioabsorbable
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