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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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Slap Hammer
ALPHANOX CO.,LTD.
5901-0132
In Commercial Distribution

  • 08806373577642 ()
5901-0132

  • External spinal fixation system
Slap Hammer Adaptor
ALPHANOX CO.,LTD.
5901-0133
In Commercial Distribution

  • 08806373577161 ()
5901-0133

  • External spinal fixation system
PEEK PLIF Cage Trial 4°
ALPHANOX CO.,LTD.
5901-4113
In Commercial Distribution

  • 08806373568657 ()
5901-4113

  • External spinal fixation system
PEEK PLIF Cage Trial 4°
ALPHANOX CO.,LTD.
5901-4111
In Commercial Distribution

  • 08806373568633 ()
5901-4111

  • External spinal fixation system
PEEK PLIF Cage Trial 4°
ALPHANOX CO.,LTD.
5901-4109
In Commercial Distribution

  • 08806373568619 ()
5901-4109

  • External spinal fixation system
PEEK PLIF Cage Trial 0°
ALPHANOX CO.,LTD.
5901-4014
In Commercial Distribution

  • 08806373568602 ()
5901-4014

  • External spinal fixation system
PEEK PLIF Cage Trial 0°
ALPHANOX CO.,LTD.
5901-4013
In Commercial Distribution

  • 08806373568596 ()
5901-4013

  • External spinal fixation system
PEEK PLIF Cage Trial 0°
ALPHANOX CO.,LTD.
5901-4012
In Commercial Distribution

  • 08806373568589 ()
5901-4012

  • External spinal fixation system
PEEK PLIF Cage Trial 0°
ALPHANOX CO.,LTD.
5901-4011
In Commercial Distribution

  • 08806373568572 ()
5901-4011

  • External spinal fixation system
PEEK PLIF Cage Trial 0°
ALPHANOX CO.,LTD.
5901-4010
In Commercial Distribution

  • 08806373568565 ()
5901-4010

  • External spinal fixation system
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