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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 Size Device Class Implantable

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RELINE C Screw, 4.0x36mm FA
Nuvasive, Inc.
3914036
In Commercial Distribution

  • 00195377069542 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x34mm FA
Nuvasive, Inc.
3914034
In Commercial Distribution

  • 00195377069535 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x32mm FA
Nuvasive, Inc.
3914032
In Commercial Distribution

  • 00195377069528 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x30mm FA
Nuvasive, Inc.
3914030
In Commercial Distribution

  • 00195377069511 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x28mm FA
Nuvasive, Inc.
3914028
In Commercial Distribution

  • 00195377069504 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x26mm FA
Nuvasive, Inc.
3914026
In Commercial Distribution

  • 00195377069498 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x24mm FA
Nuvasive, Inc.
3914024
In Commercial Distribution

  • 00195377069481 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x22mm FA
Nuvasive, Inc.
3914022
In Commercial Distribution

  • 00195377069474 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x20mm FA
Nuvasive, Inc.
3914020
In Commercial Distribution

  • 00195377069467 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE C Screw, 4.0x18mm FA
Nuvasive, Inc.
3914018
In Commercial Distribution

  • 00195377069450 ()


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