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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ARM15S Screw, 4.5X45mm PLS
Nuvasive, Inc.
8354545
In Commercial Distribution

  • 00887517234285 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X40mm PLS
Nuvasive, Inc.
8354540
In Commercial Distribution

  • 00887517234278 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X35mm PLS
Nuvasive, Inc.
8354535
In Commercial Distribution

  • 00887517234261 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X30mm PLS
Nuvasive, Inc.
8354530
In Commercial Distribution

  • 00887517234254 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4.5X25mm PLS
Nuvasive, Inc.
8354525
In Commercial Distribution

  • 00887517234247 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4X45mm PLS
Nuvasive, Inc.
8354045
In Commercial Distribution

  • 00887517234223 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4X40mm PLS
Nuvasive, Inc.
8354040
In Commercial Distribution

  • 00887517234216 ()


  • Bone-screw internal spinal fixation system, non-sterile
ARM15S Screw, 4X35mm PLS
Nuvasive, Inc.
8354035
In Commercial Distribution

  • 00887517234209 ()


  • Bone-screw internal spinal fixation system, non-sterile
Armada Ti 3CO Impactor, 15mm Lumbar
Nuvasive, Inc.
8992121
In Commercial Distribution

  • 00887517233998 ()


  • Orthopaedic implant impactor, reusable
Armada Ti 3CO Impactor, 10mm Lumbar
Nuvasive, Inc.
8992120
In Commercial Distribution

  • 00887517233981 ()


  • Orthopaedic implant impactor, reusable
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