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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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CoRoent - 00887517889935

CoRoent Ant TLIF PEEK, 12x9x32mm 12°
Nuvasive, Inc.
5129322P2
In Commercial Distribution

  • 00887517889935 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889928

CoRoent Ant TLIF PEEK, 12x9x32mm 0°
Nuvasive, Inc.
5129320P2
In Commercial Distribution

  • 00887517889928 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889911

CoRoent Ant TLIF PEEK, 12x9x30mm 15°
Nuvasive, Inc.
5129305P2
In Commercial Distribution

  • 00887517889911 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889904

CoRoent Ant TLIF PEEK, 12x9x30mm 4°
Nuvasive, Inc.
5129304P2
In Commercial Distribution

  • 00887517889904 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889898

CoRoent Ant TLIF PEEK, 12x9x30mm 0°
Nuvasive, Inc.
5129300P2
In Commercial Distribution

  • 00887517889898 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889881

CoRoent Ant TLIF PEEK, 12x9x28mm 8°
Nuvasive, Inc.
5129288P2
In Commercial Distribution

  • 00887517889881 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889874

CoRoent Ant TLIF PEEK, 12x9x28mm 15°
Nuvasive, Inc.
5129285P2
In Commercial Distribution

  • 00887517889874 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889867

CoRoent Ant TLIF PEEK, 12x9x28mm 4°
Nuvasive, Inc.
5129284P2
In Commercial Distribution

  • 00887517889867 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889850

CoRoent Ant TLIF PEEK, 12x9x28mm 12°
Nuvasive, Inc.
5129282P2
In Commercial Distribution

  • 00887517889850 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517889843

CoRoent Ant TLIF PEEK, 12x9x28mm 0°
Nuvasive, Inc.
5129280P2
In Commercial Distribution

  • 00887517889843 ()


  • Metallic spinal interbody fusion cage
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