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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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CoRoent - 00887517823090

Interlock II Trial, 10x17x14mm 20°
Nuvasive, Inc.
6774210
In Commercial Distribution

  • 00887517823090 ()


  • Spinal implant trial

CoRoent - 00887517823083

Interlock II Trial, 9x17x14mm 20°
Nuvasive, Inc.
6774209
In Commercial Distribution

  • 00887517823083 ()


  • Spinal implant trial

CoRoent - 00887517823076

Interlock II Trial, 8x17x14mm 20°
Nuvasive, Inc.
6774208
In Commercial Distribution

  • 00887517823076 ()


  • Spinal implant trial

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 - 00887517836182

BASE Trial Rasp, 10x42x30mm 20°
Nuvasive, Inc.
6956996
In Commercial Distribution

  • 00887517836182 ()


  • Spinal implant trial

ALIF - 00887517836175

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

  • 00887517836175 ()


  • Spinal implant trial

ALIF - 00887517836168

BASE Trial Rasp, 6x42x30mm 20°
Nuvasive, Inc.
6956994
In Commercial Distribution

  • 00887517836168 ()


  • Spinal implant trial
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