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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RELINE-C Ti Rod, 4.0x85mm Pre-Bent
Nuvasive, Inc.
3744085
In Commercial Distribution

  • 00887517003911 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x80mm Pre-Bent
Nuvasive, Inc.
3744080
In Commercial Distribution

  • 00887517003904 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x75mm Pre-Bent
Nuvasive, Inc.
3744075
In Commercial Distribution

  • 00887517003898 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x70mm Pre-Bent
Nuvasive, Inc.
3744070
In Commercial Distribution

  • 00887517003881 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x65mm Pre-Bent
Nuvasive, Inc.
3744065
In Commercial Distribution

  • 00887517003874 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x60mm Pre-Bent
Nuvasive, Inc.
3744060
In Commercial Distribution

  • 00887517003867 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x55mm Pre-Bent
Nuvasive, Inc.
3744055
In Commercial Distribution

  • 00887517003850 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x50mm Pre-Bent
Nuvasive, Inc.
3744050
In Commercial Distribution

  • 00887517003843 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x45mm Pre-Bent
Nuvasive, Inc.
3744045
In Commercial Distribution

  • 00887517003836 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Ti Rod, 4.0x40mm Pre-Bent
Nuvasive, Inc.
3744040
In Commercial Distribution

  • 00887517003829 ()


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