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 Class Implantable

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VuePoint II Conn, 30mmx35° LateralOffset
Nuvasive, Inc.
8976031P3
In Commercial Distribution

  • 00887517830364 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Conn, 30mmx45° LateralOffset
Nuvasive, Inc.
8976030P3
In Commercial Distribution

  • 00887517830340 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Conn, 25mmx0° Lateral Offset
Nuvasive, Inc.
8976025P3
In Commercial Distribution

  • 00887517830326 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Conn, 20mmx0° Lateral Offset
Nuvasive, Inc.
8976020P3
In Commercial Distribution

  • 00887517830302 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Conn, 15mmx0° Lateral Offset
Nuvasive, Inc.
8976015P3
In Commercial Distribution

  • 00887517830289 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Conn, 11mmx0° Lateral Offset
Nuvasive, Inc.
8976011P3
In Commercial Distribution

  • 00887517830265 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Cross Conn, Adj Tulip-Tulip
Nuvasive, Inc.
8972360P3
In Commercial Distribution

  • 00887517829078 ()


  • Bone-screw internal spinal fixation system, sterile
VuePoint II Set Screw, Tulip&LaminarHook
Nuvasive, Inc.
8970000P3
In Commercial Distribution

  • 00887517829054 ()


  • Bone-screw internal spinal fixation system, sterile
Modulus XLXW, 8x26x60mm 5°
Nuvasive, Inc.
1263860P2
In Commercial Distribution

  • 00887517828996 ()


  • Metallic spinal interbody fusion cage
Modulus XLXW, 8x26x55mm 5°
Nuvasive, Inc.
1263855P2
In Commercial Distribution

  • 00887517828972 ()


  • Metallic spinal interbody fusion cage
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