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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SpheRx® DBR® III Rod, 62.5mm DB Pre-Bent
Nuvasive, Inc.
7237625
In Commercial Distribution

  • 00887517439406 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 60.0mm DB Pre-Bent
Nuvasive, Inc.
7237600
In Commercial Distribution

  • 00887517439093 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 57.5mm DB Pre-Bent
Nuvasive, Inc.
7237575
In Commercial Distribution

  • 00887517439086 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 55mm DB Pre-Bent
Nuvasive, Inc.
7237550
In Commercial Distribution

  • 00887517439079 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 52.5mm DB Pre-Bent
Nuvasive, Inc.
7237525
In Commercial Distribution

  • 00887517439062 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 50mm DB Pre-Bent
Nuvasive, Inc.
7237500
In Commercial Distribution

  • 00887517439055 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 47.5mm DB Pre-Bent
Nuvasive, Inc.
7237475
In Commercial Distribution

  • 00887517439048 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 45mm DB Pre-Bent
Nuvasive, Inc.
7237450
In Commercial Distribution

  • 00887517439031 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 42.5mm DB Pre-Bent
Nuvasive, Inc.
7237425
In Commercial Distribution

  • 00887517439024 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 40mm DB Pre-Bent
Nuvasive, Inc.
7237400
In Commercial Distribution

  • 00887517439017 ()


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