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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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BASE - 00887517722461

BASE Ti HL Implant, 12x42x32mm 20°
Nuvasive, Inc.
6959178
In Commercial Distribution

  • 00887517722461 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517722454

BASE Ti HL Implant, 10x42x32mm 20°
Nuvasive, Inc.
6959177
In Commercial Distribution

  • 00887517722454 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517722447

BASE Ti HL Implant, 8x42x32mm 20°
Nuvasive, Inc.
6959176
In Commercial Distribution

  • 00887517722447 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517722430

BASE Ti HL Implant, 6x42x32mm 20°
Nuvasive, Inc.
6959175
In Commercial Distribution

  • 00887517722430 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517712219

CoRoent Small ACR Trial, 16x22x19mm 20°
Nuvasive, Inc.
6725436
In Commercial Distribution

  • 00887517712219 ()


  • Spinal implant trial

CoRoent - 00887517712202

CoRoent Small ACR Trial, 15x22x19mm 20°
Nuvasive, Inc.
6725435
In Commercial Distribution

  • 00887517712202 ()


  • Spinal implant trial

CoRoent - 00887517712196

CoRoent Small ACR Trial, 14x22x19mm 20°
Nuvasive, Inc.
6725434
In Commercial Distribution

  • 00887517712196 ()


  • Spinal implant trial

CoRoent - 00887517712189

CoRoent Small ACR Trial, 13x22x19mm 20°
Nuvasive, Inc.
6725433
In Commercial Distribution

  • 00887517712189 ()


  • Spinal implant trial

CoRoent - 00887517712172

CoRoent Small ACR Trial, 12x22x19mm 20°
Nuvasive, Inc.
6725432
In Commercial Distribution

  • 00887517712172 ()


  • Spinal implant trial

CoRoent - 00887517712165

CoRoent Small ACR Trial, 11x22x19mm 20°
Nuvasive, Inc.
6725431
In Commercial Distribution

  • 00887517712165 ()


  • Spinal implant trial
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