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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 - 00887517835550

BASE Trial Rasp, 4x38x32mm 20°
Nuvasive, Inc.
6956933
In Commercial Distribution

  • 00887517835550 ()


  • Spinal implant trial

ALIF - 00887517835307

BASE Trial Rasp, 14x38x28mm 20°
Nuvasive, Inc.
6956908
In Commercial Distribution

  • 00887517835307 ()


  • Spinal implant trial

ALIF - 00887517835291

BASE Trial Rasp, 12x38x28mm 20°
Nuvasive, Inc.
6956907
In Commercial Distribution

  • 00887517835291 ()


  • Spinal implant trial

ALIF - 00887517835284

BASE Trial Rasp, 10x38x28mm 20°
Nuvasive, Inc.
6956906
In Commercial Distribution

  • 00887517835284 ()


  • Spinal implant trial

ALIF - 00887517835277

BASE Trial Rasp, 8x38x28mm 20°
Nuvasive, Inc.
6956905
In Commercial Distribution

  • 00887517835277 ()


  • Spinal implant trial

ALIF - 00887517835260

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

  • 00887517835260 ()


  • Spinal implant trial

ALIF - 00887517835253

BASE Trial Rasp, 4x38x28mm 20°
Nuvasive, Inc.
6956903
In Commercial Distribution

  • 00887517835253 ()


  • 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
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