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® II Screw, 7.5 x 45mm Double Lead
Nuvasive, Inc.
7197545
In Commercial Distribution

  • 00887517428660 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Screw, 7.5 x 40mm Double Lead
Nuvasive, Inc.
7197540
In Commercial Distribution

  • 00887517428653 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Screw, 7.5 x 35mm Double Lead
Nuvasive, Inc.
7197535
In Commercial Distribution

  • 00887517428646 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Screw, 6.5 x 55mm Double Lead
Nuvasive, Inc.
7196555
In Commercial Distribution

  • 00887517428639 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Screw, 6.5 x 50mm Double Lead
Nuvasive, Inc.
7196550
In Commercial Distribution

  • 00887517428622 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Screw, 6.5 x 45mm Double Lead
Nuvasive, Inc.
7196545
In Commercial Distribution

  • 00887517428615 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® II Screw, 6.5x40mm Double Lead
Nuvasive, Inc.
7196540
In Commercial Distribution

  • 00887517428608 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 120mm Pre-Bent
Nuvasive, Inc.
7217120
In Commercial Distribution

  • 00887517433497 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 110mm Pre-Bent
Nuvasive, Inc.
7217110
In Commercial Distribution

  • 00887517433480 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 105mm Pre-Bent
Nuvasive, Inc.
7217105
In Commercial Distribution

  • 00887517433473 ()


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