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 Class Implantable

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CoRoent® SI, 12x19x16mm 10° Ta
Nuvasive, Inc.
6790532
In Commercial Distribution

  • 00887517205810 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 11x19x16mm 10° Ta
Nuvasive, Inc.
6790531
In Commercial Distribution

  • 00887517205803 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 10x19x16mm 10° Ta
Nuvasive, Inc.
6790530
In Commercial Distribution

  • 00887517205599 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 9x19x16mm 10° Ta
Nuvasive, Inc.
6790529
In Commercial Distribution

  • 00887517205582 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 8x19x16mm 10° Ta
Nuvasive, Inc.
6790528
In Commercial Distribution

  • 00887517205575 ()


  • Polymeric spinal interbody fusion cage
CoRoent® SI, 7x19x16mm 10° Ta
Nuvasive, Inc.
6790527
In Commercial Distribution

  • 00887517205568 ()


  • Polymeric spinal interbody fusion cage
CoRoent LC, 16x11x30mm 8°
Nuvasive, Inc.
6616130
In Commercial Distribution

  • 00887517203465 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LC, 14x9x30mm 8°
Nuvasive, Inc.
6614930
In Commercial Distribution

  • 00887517203403 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LC, 14x11x30mm 8°
Nuvasive, Inc.
6614130
In Commercial Distribution

  • 00887517202987 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LC, 13x9x30mm 8°
Nuvasive, Inc.
6613930
In Commercial Distribution

  • 00887517202963 ()


  • Polymeric spinal interbody fusion cage
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