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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 - 00887517834652

BASE Trial Rasp, 4x34x24mm 20°
Nuvasive, Inc.
6956843
In Commercial Distribution

  • 00887517834652 ()


  • Spinal implant trial

TLX - 00887517826206

TLX Inner Rod, 20° 36mm
Nuvasive, Inc.
1788336
In Commercial Distribution

  • 00887517826206 ()


  • Internal spinal fixation procedure kit, reusable

TLX - 00887517826190

TLX Inner Rod, 20° 31mm
Nuvasive, Inc.
1788331
In Commercial Distribution

  • 00887517826190 ()


  • Surgical implant/trial-implant/sizer holder, reusable

TLX - 00887517826183

TLX Inner Rod, 20° 26mm
Nuvasive, Inc.
1788326
In Commercial Distribution

  • 00887517826183 ()


  • Surgical implant/trial-implant/sizer holder, reusable

CoRoent - 00887517823144

Interlock II Trial, 15x17x14mm 20°
Nuvasive, Inc.
6774215
In Commercial Distribution

  • 00887517823144 ()


  • Spinal implant trial

CoRoent - 00887517823120

Interlock II Trial, 13x17x14mm 20°
Nuvasive, Inc.
6774213
In Commercial Distribution

  • 00887517823120 ()


  • Spinal implant trial

CoRoent - 00887517823106

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

  • 00887517823106 ()


  • Spinal implant trial

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
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