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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Interlock II Trial, 11x17x14mm 20°
Nuvasive, Inc.
6774211
In Commercial Distribution

  • 00887517823106 ()


  • Spinal implant trial
Interlock II Trial, 10x17x14mm 20°
Nuvasive, Inc.
6774210
In Commercial Distribution

  • 00887517823090 ()


  • Spinal implant trial
Interlock II Trial, 9x17x14mm 20°
Nuvasive, Inc.
6774209
In Commercial Distribution

  • 00887517823083 ()


  • Spinal implant trial
Interlock II Trial, 8x17x14mm 20°
Nuvasive, Inc.
6774208
In Commercial Distribution

  • 00887517823076 ()


  • Spinal implant trial
BASE Trial Rasp, 14x42x30mm 20°
Nuvasive, Inc.
6956998
In Commercial Distribution

  • 00887517836205 ()


  • Spinal implant trial
BASE Trial Rasp, 12x42x30mm 20°
Nuvasive, Inc.
6956997
In Commercial Distribution

  • 00887517836199 ()


  • Spinal implant trial
BASE Trial Rasp, 10x42x30mm 20°
Nuvasive, Inc.
6956996
In Commercial Distribution

  • 00887517836182 ()


  • Spinal implant trial
BASE Trial Rasp, 8x42x30mm 20°
Nuvasive, Inc.
6956995
In Commercial Distribution

  • 00887517836175 ()


  • Spinal implant trial
BASE Trial Rasp, 6x42x30mm 20°
Nuvasive, Inc.
6956994
In Commercial Distribution

  • 00887517836168 ()


  • Spinal implant trial
BASE Trial Rasp, 4x42x30mm 20°
Nuvasive, Inc.
6956993
In Commercial Distribution

  • 00887517836151 ()


  • Spinal implant trial
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