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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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ALIF - 00887517835260

BASE Trial Rasp, 6x38x28mm 20°
Nuvasive, Inc.
6956904
In Commercial Distribution

  • 00887517835260 ()


  • Spinal implant trial

ALIF - 00887517835000

BASE Trial Rasp, 14x34x28mm 20°
Nuvasive, Inc.
6956878
In Commercial Distribution

  • 00887517835000 ()


  • Spinal implant trial

ALIF - 00887517834997

BASE Trial Rasp, 12x34x28mm 20°
Nuvasive, Inc.
6956877
In Commercial Distribution

  • 00887517834997 ()


  • Spinal implant trial

ALIF - 00887517834980

BASE Trial Rasp, 10x34x28mm 20°
Nuvasive, Inc.
6956876
In Commercial Distribution

  • 00887517834980 ()


  • Spinal implant trial

ALIF - 00887517834973

BASE Trial Rasp, 8x34x28mm 20°
Nuvasive, Inc.
6956875
In Commercial Distribution

  • 00887517834973 ()


  • Spinal implant trial

ALIF - 00887517834966

BASE Trial Rasp, 6x34x28mm 20°
Nuvasive, Inc.
6956874
In Commercial Distribution

  • 00887517834966 ()


  • Spinal implant trial

ALIF - 00887517834959

BASE Trial Rasp, 4x34x28mm 20°
Nuvasive, Inc.
6956873
In Commercial Distribution

  • 00887517834959 ()


  • Spinal implant trial

ALIF - 00887517834706

BASE Trial Rasp, 14x34x24mm 20°
Nuvasive, Inc.
6956848
In Commercial Distribution

  • 00887517834706 ()


  • Spinal implant trial

ALIF - 00887517834690

BASE Trial Rasp, 12x34x24mm 20°
Nuvasive, Inc.
6956847
In Commercial Distribution

  • 00887517834690 ()


  • Spinal implant trial

ALIF - 00887517834683

BASE Trial Rasp, 10x34x24mm 20°
Nuvasive, Inc.
6956846
In Commercial Distribution

  • 00887517834683 ()


  • Spinal implant trial
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