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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 - 00887517702630

BASE Ti HL Implant, 14x34x28mm 20°
Nuvasive, Inc.
6959014
In Commercial Distribution

  • 00887517702630 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517702623

BASE Ti HL Implant, 12x34x28mm 20°
Nuvasive, Inc.
6959013
In Commercial Distribution

  • 00887517702623 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517702616

BASE Ti HL Implant, 10x34x28mm 20°
Nuvasive, Inc.
6959012
In Commercial Distribution

  • 00887517702616 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517702609

BASE Ti HL Implant, 8x34x28mm 20°
Nuvasive, Inc.
6959011
In Commercial Distribution

  • 00887517702609 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517702593

BASE Ti HL Implant, 6x34x28mm 20°
Nuvasive, Inc.
6959010
In Commercial Distribution

  • 00887517702593 ()


  • Metallic spinal interbody fusion cage

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
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