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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 Class Implantable

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RELINE-C Screw, 4.0x28mm FA
Nuvasive, Inc.
3814028
In Commercial Distribution

  • 00195377017932 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x26mm FA
Nuvasive, Inc.
3814026
In Commercial Distribution

  • 00195377017925 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x24mm FA
Nuvasive, Inc.
3814024
In Commercial Distribution

  • 00195377017918 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x22mm FA
Nuvasive, Inc.
3814022
In Commercial Distribution

  • 00195377017901 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x20mm FA
Nuvasive, Inc.
3814020
In Commercial Distribution

  • 00195377017895 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x18mm FA
Nuvasive, Inc.
3814018
In Commercial Distribution

  • 00195377017888 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x16mm FA
Nuvasive, Inc.
3814016
In Commercial Distribution

  • 00195377017871 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x14mm FA
Nuvasive, Inc.
3814014
In Commercial Distribution

  • 00195377017864 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x12mm FA
Nuvasive, Inc.
3814012
In Commercial Distribution

  • 00195377017857 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-C Screw, 4.0x10mm FA
Nuvasive, Inc.
3814010
In Commercial Distribution

  • 00195377017840 ()


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