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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 Class Implantable

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CoRoent - 00887517391773

CoRoent® XL Wide, 12x22x50mm
Nuvasive, Inc.
6912250
In Commercial Distribution

  • 00887517391773 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517391766

CoRoent® XL Wide, 12x22x45mm
Nuvasive, Inc.
6912245
In Commercial Distribution

  • 00887517391766 ()


  • Polymeric spinal interbody fusion cage

Armada - 00887517391490

ARM15S Screw, 4.5x30mm Fixed
Nuvasive, Inc.
8954530
In Commercial Distribution

  • 00887517391490 ()


  • Bone-screw internal spinal fixation system, non-sterile

Armada - 00887517391483

ARM15S Screw, 4.5x25mm Fixed
Nuvasive, Inc.
8954525
In Commercial Distribution

  • 00887517391483 ()


  • Bone-screw internal spinal fixation system, non-sterile

Armada - 00887517391469

ARM15S Screw, 4x40mm Fixed
Nuvasive, Inc.
8954040
In Commercial Distribution

  • 00887517391469 ()


  • Bone-screw internal spinal fixation system, non-sterile

Armada - 00887517391438

ARM15S Screw, 4x25mm Fixed
Nuvasive, Inc.
8954025
In Commercial Distribution

  • 00887517391438 ()


  • Bone-screw internal spinal fixation system, non-sterile

Brigade - 00887517391421

CoRoent XLR-F, 16x42x30mm 12°
Nuvasive, Inc.
8931642
In Commercial Distribution

  • 00887517391421 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517391414

CoRoent XLR-F, 16x38x28mm 12°
Nuvasive, Inc.
8931638
In Commercial Distribution

  • 00887517391414 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517391407

CoRoent XLR-F, 16x34x24mm 12°
Nuvasive, Inc.
8931634
In Commercial Distribution

  • 00887517391407 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517391391

CoRoent® XL, 10x18x60mm
Nuvasive, Inc.
6910860
In Commercial Distribution

  • 00887517391391 ()


  • Polymeric spinal interbody fusion cage
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