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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 Class Implantable

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VuePoint - 00887517932020

VuePoint II Drill Bit, 2.4mm OUS
Nuvasive, Inc.
8976113
In Commercial Distribution

  • 00887517932020 ()


  • Cannulated surgical drill bit, reusable

NuVasive - 00887517913340

Universal Ring Curette Left Angled - Jp
Nuvasive, Inc.
7175025
In Commercial Distribution

  • 00887517913340 ()


  • Neurosurgical curette, single-use

NuVasive - 00887517913333

Universal Ring Curette Right Angled -Jp
Nuvasive, Inc.
7175024
In Commercial Distribution

  • 00887517913333 ()


  • Neurosurgical curette, single-use

NuVasive - 00887517913326

Universal Ring Curette Straight - Japan
Nuvasive, Inc.
7175023
In Commercial Distribution

  • 00887517913326 ()


  • Neurosurgical curette, single-use

NuVasive - 00887517913319

Universal Bone Graft Tamp - Japan
Nuvasive, Inc.
7175022
In Commercial Distribution

  • 00887517913319 ()


  • Surgical tamp, reusable

CoRoent - 00195377016997

CoRoent XLR Trial, 6x26x22mm 10° Detach
Nuvasive, Inc.
6970662
In Commercial Distribution

  • 00195377016997 ()


  • Internal spinal fixation procedure kit, reusable

CoRoent - 00195377006448

CoRoent SI Drill Bit, 2.0x12mm
Nuvasive, Inc.
6790151P
In Commercial Distribution

  • 00195377006448 ()


  • Internal spinal fixation procedure kit, single-use

VuePoint - 00195377003799

NAV.S VuePoint II Drill Bit
Nuvasive, Inc.
8801610P
In Commercial Distribution

  • 00195377003799 ()


  • Internal spinal fixation procedure kit, single-use

VuePoint - 00195377003492

VuePoint II Template, 120mm Rod
Nuvasive, Inc.
8970120P
In Commercial Distribution

  • 00195377003492 ()


  • Internal spinal fixation procedure kit, single-use

VuePoint - 00195377003379

VuePoint II Drill Bit
Nuvasive, Inc.
8977010P
In Commercial Distribution

  • 00195377003379 ()


  • Internal spinal fixation procedure kit, single-use
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