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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Parallel guide Ø4 - Ø4
NOVASTEP
XMS01038-6
In Commercial Distribution

  • 03700879513997 ()
XMS01038-6

  • General internal orthopaedic fixation system implantation kit
Parallel guide Ø4 - Ø3
NOVASTEP
XMS01038-5
In Commercial Distribution

  • 03700879513980 ()
XMS01038-5

  • General internal orthopaedic fixation system implantation kit
cutting template - Left
NOVASTEP
XMS01040-2
In Commercial Distribution

  • 03700879513973 ()
XMS01040-2

  • General internal orthopaedic fixation system implantation kit
cutting template - Right
NOVASTEP
XMS01040-1
In Commercial Distribution

  • 03700879513966 ()
XMS01040-1

  • General internal orthopaedic fixation system implantation kit
airlock® Talonavicular Jig holder
NOVASTEP
ACC1006P0014
Not in Commercial Distribution

  • 03700879513959 ()
ACC1006P0014

  • Device sterilization/disinfection container, reusable
Airlock® Lapidus Jig holder
NOVASTEP
ACC1006P0013
Not in Commercial Distribution

  • 03700879513942 ()
ACC1006P0013

  • Device sterilization/disinfection container, reusable
Airlock® K-wire sleeve for Lapidus targeting guide
NOVASTEP
XMS01037-3
Not in Commercial Distribution

  • 03700879513935 ()
XMS01037-3

  • General internal orthopaedic fixation system implantation kit
Lapidus targeting guide - Left
NOVASTEP
XMS01037-2
Not in Commercial Distribution

  • 03700879513928 ()
XMS01037-2

  • General internal orthopaedic fixation system implantation kit
Airlock® Lapidus targeting guide - Right
NOVASTEP
XMS01037-1
Not in Commercial Distribution

  • 03700879513911 ()
XMS01037-1

  • General internal orthopaedic fixation system implantation kit
Airlock K-wire sleeve for TN targeting guide
NOVASTEP
XMS01039-3
Not in Commercial Distribution

  • 03700879513904 ()
XMS01039-3

  • General internal orthopaedic fixation system implantation kit
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