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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 - 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 - 00887517835604

BASE Trial Rasp, 14x38x32mm 20°
Nuvasive, Inc.
6956938
In Commercial Distribution

  • 00887517835604 ()


  • Spinal implant trial

ALIF - 00887517835598

BASE Trial Rasp, 12x38x32mm 20°
Nuvasive, Inc.
6956937
In Commercial Distribution

  • 00887517835598 ()


  • Spinal implant trial

ALIF - 00887517835581

BASE Trial Rasp, 10x38x32mm 20°
Nuvasive, Inc.
6956936
In Commercial Distribution

  • 00887517835581 ()


  • Spinal implant trial

ALIF - 00887517835574

BASE Trial Rasp, 8x38x32mm 20°
Nuvasive, Inc.
6956935
In Commercial Distribution

  • 00887517835574 ()


  • Spinal implant trial

ALIF - 00887517835567

BASE Trial Rasp, 6x38x32mm 20°
Nuvasive, Inc.
6956934
In Commercial Distribution

  • 00887517835567 ()


  • Spinal implant trial
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