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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 - 00887517683854

CoRoent LO, 10x10x35mm 5°
Nuvasive, Inc.
6851012P2
In Commercial Distribution

  • 00887517683854 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517683830

CoRoent LO, 10x10x30mm 5°
Nuvasive, Inc.
6851011P2
In Commercial Distribution

  • 00887517683830 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517683816

CoRoent LO, 10x10x25mm 5°
Nuvasive, Inc.
6851010P2
In Commercial Distribution

  • 00887517683816 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517683731

CoRoent LO, 8x10x35mm 5°
Nuvasive, Inc.
6850812P2
In Commercial Distribution

  • 00887517683731 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517683717

CoRoent LO, 8x10x30mm 5°
Nuvasive, Inc.
6850811P2
In Commercial Distribution

  • 00887517683717 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517683694

CoRoent LO, 8x10x25mm 5°
Nuvasive, Inc.
6850810P2
In Commercial Distribution

  • 00887517683694 ()


  • Polymeric spinal interbody fusion cage

Armada - 00887517484130

ARM16S Base, Instrument 5
Nuvasive, Inc.
7451335
In Commercial Distribution

  • 00887517484130 ()


  • Device sterilization/disinfection container, reusable

Modulus - 00887517828972

Modulus XLXW, 8x26x55mm 5°
Nuvasive, Inc.
1263855P2
In Commercial Distribution

  • 00887517828972 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828958

Modulus XLXW, 8x26x50mm 5°
Nuvasive, Inc.
1263850P2
In Commercial Distribution

  • 00887517828958 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517828996

Modulus XLXW, 8x26x60mm 5°
Nuvasive, Inc.
1263860P2
In Commercial Distribution

  • 00887517828996 ()


  • Metallic spinal interbody fusion cage
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