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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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P.L.U.S.® - 03663136024615

LAMINA FEELER
SPINEVISION
U1-A112
In Commercial Distribution

  • 03663136024615 ()

  • 0


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

P.L.U.S.® - 03663136024608

PEDICLE FEELER
SPINEVISION
U1-A111
In Commercial Distribution

  • 03663136024608 ()

  • 0


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

NA - 03663136024486

Curved rongeur 4mm
SPINEVISION
TL1 – A030
In Commercial Distribution

  • 03663136024486 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024479

Distraction plier
SPINEVISION
TL1-A029
In Commercial Distribution

  • 03663136024479 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024462

Cage support
SPINEVISION
TL1 – A028
In Commercial Distribution

  • 03663136024462 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024417

Curved rongeur 10mm
SPINEVISION
TL1-A020
In Commercial Distribution

  • 03663136024417 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024196

Graft Funnell
SPINEVISION
TL1-A009
In Commercial Distribution

  • 03663136024196 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024189

Cage Support/T
SPINEVISION
TL1-A007
In Commercial Distribution

  • 03663136024189 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024141

Curved Rongeur
SPINEVISION
TL1-A002
In Commercial Distribution

  • 03663136024141 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024134

6 Arm for PLUS
SPINEVISION
TL1-A001-5
In Commercial Distribution

  • 03663136024134 ()

  • 0


  • Polymeric spinal interbody fusion cage
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