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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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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

CoRoent - 00887517712158

CoRoent Small ACR Trial, 10x22x19mm 20°
Nuvasive, Inc.
6725430
In Commercial Distribution

  • 00887517712158 ()


  • Spinal implant trial

BASE - 00887517704764

BASE Ti HL Implant, 14x42x36mm 20°
Nuvasive, Inc.
6959234
In Commercial Distribution

  • 00887517704764 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517704757

BASE Ti HL Implant, 12x42x36mm 20°
Nuvasive, Inc.
6959233
In Commercial Distribution

  • 00887517704757 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517704726

BASE Ti HL Implant, 6x42x36mm 20°
Nuvasive, Inc.
6959230
In Commercial Distribution

  • 00887517704726 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517704214

BASE Ti HL Implant, 14x42x32mm 20°
Nuvasive, Inc.
6959179
In Commercial Distribution

  • 00887517704214 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703729

BASE Ti HL Implant, 14x38x36mm 20°
Nuvasive, Inc.
6959124
In Commercial Distribution

  • 00887517703729 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703705

BASE Ti HL Implant, 10x38x36mm 20°
Nuvasive, Inc.
6959122
In Commercial Distribution

  • 00887517703705 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703163

BASE Ti HL Implant, 10x38x32mm 20°
Nuvasive, Inc.
6959067
In Commercial Distribution

  • 00887517703163 ()


  • Metallic spinal interbody fusion cage
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