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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 - 00887517701350

BASE Ti HL Implant, 8x42x30mm 20°
Nuvasive, Inc.
6953820
In Commercial Distribution

  • 00887517701350 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701305

BASE Ti HL Implant, 6x42x30mm 20°
Nuvasive, Inc.
6953620
In Commercial Distribution

  • 00887517701305 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701251

BASE Ti HL Implant, 14x42x30mm 20°
Nuvasive, Inc.
6953420
In Commercial Distribution

  • 00887517701251 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701206

BASE Ti HL Implant, 12x42x30mm 20°
Nuvasive, Inc.
6953220
In Commercial Distribution

  • 00887517701206 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701152

BASE Ti HL Implant, 10x42x30mm 20°
Nuvasive, Inc.
6953020
In Commercial Distribution

  • 00887517701152 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701107

BASE Ti HL Implant, 8x38x28mm 20°
Nuvasive, Inc.
6952820
In Commercial Distribution

  • 00887517701107 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701053

BASE Ti HL Implant, 6x38x28mm 20°
Nuvasive, Inc.
6952620
In Commercial Distribution

  • 00887517701053 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517701008

BASE Ti HL Implant, 14x38x28mm 20°
Nuvasive, Inc.
6952420
In Commercial Distribution

  • 00887517701008 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517700957

BASE Ti HL Implant, 12x38x28mm 20°
Nuvasive, Inc.
6952220
In Commercial Distribution

  • 00887517700957 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517700902

BASE Ti HL Implant, 10x38x28mm 20°
Nuvasive, Inc.
6952020
In Commercial Distribution

  • 00887517700902 ()


  • Metallic spinal interbody fusion cage
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