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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 Size Type Device Class Implantable

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Laminar Hook 5.0mm
SPINECRAFT, LLC
H6-5050
In Commercial Distribution

  • M824H650501 ()


  • Bone-screw internal spinal fixation system
Fixed Length Cross Connector 28mm
SPINECRAFT, LLC
F6-1828
In Commercial Distribution

  • M824F618281 ()


  • Bone-screw internal spinal fixation system, non-sterile
Fixed Length Cross Connector 25mm
SPINECRAFT, LLC
F6-1825
In Commercial Distribution

  • M824F618251 ()


  • Bone-screw internal spinal fixation system, non-sterile
Fixed Length Cross Connector 22mm
SPINECRAFT, LLC
F6-1822
In Commercial Distribution

  • M824F618221 ()


  • Bone-screw internal spinal fixation system, non-sterile
Fixed Length Cross Connector 19mm
SPINECRAFT, LLC
F6-1819
In Commercial Distribution

  • M824F618191 ()


  • Bone-screw internal spinal fixation system, non-sterile
Fixed Length Cross Connector 16mm
SPINECRAFT, LLC
F6-1816
In Commercial Distribution

  • M824F618161 ()


  • Bone-screw internal spinal fixation system, non-sterile
APEX-DL Ti Uniplanar Reduction Screw 7.00 x 90mm, Self-Tapping
SPINECRAFT, LLC
DUR6-7090-F
In Commercial Distribution

  • M824DUR67090F1 ()


  • Bone-screw internal spinal fixation system, non-sterile
APEX-DL Ti Cannulated Uniplanar Reduction Screw 7.00 x 90mm, Self-Tapping
SPINECRAFT, LLC
DUR6-7090C-F
In Commercial Distribution

  • M824DUR67090CF1 ()


  • Bone-screw internal spinal fixation system, non-sterile
APEX-DL Ti Cannulated Uniplanar Reduction Screw 7.00 x 90mm
SPINECRAFT, LLC
DUR6-7090C
In Commercial Distribution

  • M824DUR67090C1 ()


  • Bone-screw internal spinal fixation system, non-sterile
APEX-DL Ti Uniplanar Reduction Screw 7.00 x 90mm
SPINECRAFT, LLC
DUR6-7090
In Commercial Distribution

  • M824DUR670901 ()


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