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

  • 00887517823076 ()


  • Spinal implant trial
BASE HL Trial, 14x42x36mm 20°
Nuvasive, Inc.
6959262
In Commercial Distribution

  • 00887517705044 ()


  • Spinal implant trial
BASE HL Trial, 12x42x36mm 20°
Nuvasive, Inc.
6959261
In Commercial Distribution

  • 00887517705037 ()


  • Spinal implant trial
BASE HL Trial, 10x42x36mm 20°
Nuvasive, Inc.
6959260
In Commercial Distribution

  • 00887517705020 ()


  • Spinal implant trial
BASE HL Trial, 6x42x36mm 20°
Nuvasive, Inc.
6959258
In Commercial Distribution

  • 00887517705006 ()


  • Spinal implant trial
BASE HL Trial, 4x42x36mm 20°
Nuvasive, Inc.
6959257
In Commercial Distribution

  • 00887517704993 ()


  • Spinal implant trial
BASE HL Trial, 12x42x32mm 20°
Nuvasive, Inc.
6959206
In Commercial Distribution

  • 00887517704481 ()


  • Spinal implant trial
BASE HL Trial, 10x42x32mm 20°
Nuvasive, Inc.
6959205
In Commercial Distribution

  • 00887517704474 ()


  • Spinal implant trial
BASE HL Trial, 8x42x32mm 20°
Nuvasive, Inc.
6959204
In Commercial Distribution

  • 00887517704467 ()


  • Spinal implant trial
BASE HL Trial, 6x42x32mm 20°
Nuvasive, Inc.
6959203
In Commercial Distribution

  • 00887517704450 ()


  • Spinal implant trial
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