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 Ant TLIF Trial 12x9x30mm 15°
Nuvasive, Inc.
5195320
In Commercial Distribution

  • 00887517640604 ()


  • Spinal implant trial
CoRoent Ant TLIF Trial 11x9x30mm 15°
Nuvasive, Inc.
5195319
In Commercial Distribution

  • 00887517640598 ()


  • Spinal implant trial
CoRoent Ant TLIF PEEK, 8x13x32mm 12°
Nuvasive, Inc.
5183322
In Commercial Distribution

  • 00887517639042 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x13x30mm 12°
Nuvasive, Inc.
5183302
In Commercial Distribution

  • 00887517639028 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x13x28mm 15°
Nuvasive, Inc.
5183285
In Commercial Distribution

  • 00887517639011 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x12x32mm 15°
Nuvasive, Inc.
5182325
In Commercial Distribution

  • 00887517638977 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x12x28mm 15°
Nuvasive, Inc.
5182285
In Commercial Distribution

  • 00887517638939 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x11x34mm 15°
Nuvasive, Inc.
5181345
In Commercial Distribution

  • 00887517638915 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x11x34mm 12°
Nuvasive, Inc.
5181342
In Commercial Distribution

  • 00887517638908 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF PEEK, 8x11x32mm 15°
Nuvasive, Inc.
5181325
In Commercial Distribution

  • 00887517638892 ()


  • Polymeric spinal interbody fusion cage
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