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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 - 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 - 00887517823939

Interlock II Trial, 16x19x16mm 20°
Nuvasive, Inc.
6777216
In Commercial Distribution

  • 00887517823939 ()


  • Spinal implant trial

CoRoent - 00887517823915

Interlock II Trial, 14x19x16mm 20°
Nuvasive, Inc.
6777214
In Commercial Distribution

  • 00887517823915 ()


  • Spinal implant trial

CoRoent - 00887517823892

Interlock II Trial, 12x19x16mm 20°
Nuvasive, Inc.
6777212
In Commercial Distribution

  • 00887517823892 ()


  • Spinal implant trial

CoRoent - 00887517823861

Interlock II Trial, 9x19x16mm 20°
Nuvasive, Inc.
6777209
In Commercial Distribution

  • 00887517823861 ()


  • Spinal implant trial

CoRoent - 00887517813374

Interlock II Ti-C, 11x19x16mm 20°
Nuvasive, Inc.
6779120CP2
In Commercial Distribution

  • 00887517813374 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813329

Interlock II Ti-C, 10x19x16mm 20°
Nuvasive, Inc.
6779020CP2
In Commercial Distribution

  • 00887517813329 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813282

Interlock II Ti-C, 9x19x16mm 20°
Nuvasive, Inc.
6778920CP2
In Commercial Distribution

  • 00887517813282 ()


  • Polymeric spinal interbody fusion cage
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