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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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BASE - 00887517705037

BASE HL Trial, 12x42x36mm 20°
Nuvasive, Inc.
6959261
In Commercial Distribution

  • 00887517705037 ()


  • Spinal implant trial

BASE - 00887517705020

BASE HL Trial, 10x42x36mm 20°
Nuvasive, Inc.
6959260
In Commercial Distribution

  • 00887517705020 ()


  • Spinal implant trial

BASE - 00887517705006

BASE HL Trial, 6x42x36mm 20°
Nuvasive, Inc.
6959258
In Commercial Distribution

  • 00887517705006 ()


  • Spinal implant trial

BASE - 00887517704993

BASE HL Trial, 4x42x36mm 20°
Nuvasive, Inc.
6959257
In Commercial Distribution

  • 00887517704993 ()


  • Spinal implant trial

BASE - 00887517703996

BASE HL Trial, 12x38x36mm 20°
Nuvasive, Inc.
6959151
In Commercial Distribution

  • 00887517703996 ()


  • Spinal implant trial

BASE - 00887517703989

BASE HL Trial, 10x38x36mm 20°
Nuvasive, Inc.
6959150
In Commercial Distribution

  • 00887517703989 ()


  • Spinal implant trial

BASE - 00887517703965

BASE HL Trial, 6x38x36mm 20°
Nuvasive, Inc.
6959148
In Commercial Distribution

  • 00887517703965 ()


  • Spinal implant trial

BASE - 00887517703958

BASE HL Trial, 4x38x36mm 20°
Nuvasive, Inc.
6959147
In Commercial Distribution

  • 00887517703958 ()


  • Spinal implant trial

BASE - 00887517702319

BASE HL Trial, 4x42x30mm 20°
Nuvasive, Inc.
6956420
In Commercial Distribution

  • 00887517702319 ()


  • Spinal implant trial

BASE - 00887517702265

BASE HL Trial, 14x42x30mm 20°
Nuvasive, Inc.
6956320
In Commercial Distribution

  • 00887517702265 ()


  • Spinal implant trial
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