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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 - 00887517836151

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

  • 00887517836151 ()


  • Spinal implant trial

ALIF - 00887517835871

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

  • 00887517835871 ()


  • Spinal implant trial

ALIF - 00887517835864

BASE Trial Rasp, 6x38x36mm 20°
Nuvasive, Inc.
6956964
In Commercial Distribution

  • 00887517835864 ()


  • Spinal implant trial

ALIF - 00887517835857

BASE Trial Rasp, 4x38x36mm 20°
Nuvasive, Inc.
6956963
In Commercial Distribution

  • 00887517835857 ()


  • Spinal implant trial

ALIF - 00887517835307

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

  • 00887517835307 ()


  • 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 - 00887517835253

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

  • 00887517835253 ()


  • Spinal implant trial

CoRoent - 00887517823939

Interlock II Trial, 16x19x16mm 20°
Nuvasive, Inc.
6777216
In Commercial Distribution

  • 00887517823939 ()


  • Spinal implant trial

CoRoent - 00887517823922

Interlock II Trial, 15x19x16mm 20°
Nuvasive, Inc.
6777215
In Commercial Distribution

  • 00887517823922 ()


  • Spinal implant trial
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