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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 - 00887517836465

BASE Trial Rasp, 6x42x32mm 20°
Nuvasive, Inc.
6957024
In Commercial Distribution

  • 00887517836465 ()


  • Spinal implant trial

ALIF - 00887517836458

BASE Trial Rasp, 4x42x32mm 20°
Nuvasive, Inc.
6957023
In Commercial Distribution

  • 00887517836458 ()


  • Spinal implant trial

ALIF - 00887517836205

BASE Trial Rasp, 14x42x30mm 20°
Nuvasive, Inc.
6956998
In Commercial Distribution

  • 00887517836205 ()


  • Spinal implant trial

ALIF - 00887517836199

BASE Trial Rasp, 12x42x30mm 20°
Nuvasive, Inc.
6956997
In Commercial Distribution

  • 00887517836199 ()


  • Spinal implant trial

ALIF - 00887517836175

BASE Trial Rasp, 8x42x30mm 20°
Nuvasive, Inc.
6956995
In Commercial Distribution

  • 00887517836175 ()


  • Spinal implant trial

ALIF - 00887517836151

BASE Trial Rasp, 4x42x30mm 20°
Nuvasive, Inc.
6956993
In Commercial Distribution

  • 00887517836151 ()


  • Spinal implant trial

ALIF - 00887517835901

BASE Trial Rasp, 14x38x36mm 20°
Nuvasive, Inc.
6956968
In Commercial Distribution

  • 00887517835901 ()


  • Spinal implant trial

ALIF - 00887517835895

BASE Trial Rasp, 12x38x36mm 20°
Nuvasive, Inc.
6956967
In Commercial Distribution

  • 00887517835895 ()


  • Spinal implant trial

ALIF - 00887517835888

BASE Trial Rasp, 10x38x36mm 20°
Nuvasive, Inc.
6956966
In Commercial Distribution

  • 00887517835888 ()


  • Spinal implant trial

ALIF - 00887517835871

BASE Trial Rasp, 8x38x36mm 20°
Nuvasive, Inc.
6956965
In Commercial Distribution

  • 00887517835871 ()


  • Spinal implant trial
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