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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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Pilon Fusion, Backpack Guide, Left
Paragon 28, Inc.
P51-926-5003
In Commercial Distribution

  • 00889795146441 ()
P51-926-5003

  • Surgical drill guide, reusable
Pilon Fusion, Caddy Lid
Paragon 28, Inc.
P50-900-PFCL
In Commercial Distribution

  • 00889795146434 ()
P50-900-PFCL

  • Device sterilization/disinfection container, reusable
Pilon Fusion, Tray Base
Paragon 28, Inc.
P50-900-PFIC
In Commercial Distribution

  • 00889795146427 ()
P50-900-PFIC

  • Device sterilization/disinfection container, reusable
Pilon Fusion, Caddy Base, Plates
Paragon 28, Inc.
P50-900-PFPC
In Commercial Distribution

  • 00889795146410 ()
P50-900-PFPC

  • Device sterilization/disinfection container, reusable
Pilon Fusion, Reciprocating Rasp
Paragon 28, Inc.
P51-926-7001
In Commercial Distribution

  • 00889795146175 ()
P51-926-7001

  • Bone file/rasp, manual, reusable
Pilon Fusion, Plate Handle
Paragon 28, Inc.
P51-926-6001
In Commercial Distribution

  • 00889795146168 ()
P51-926-6001

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Pilon Fusion, Attachment Rod
Paragon 28, Inc.
P51-926-5002
In Commercial Distribution

  • 00889795146151 ()
P51-926-5002

  • Device control handling knob
Pilon Fusion, Backpack Guide, Right
Paragon 28, Inc.
P51-926-5001
In Commercial Distribution

  • 00889795146144 ()
P51-926-5001

  • Surgical drill guide, reusable
Pilon Fusion, King Cobra Cartilage Removal Tool
Paragon 28, Inc.
P51-926-4001
In Commercial Distribution

  • 00889795146137 ()
P51-926-4001

  • Cartilage knife
Pilon Fusion, K-Wire Guide, Monster
Paragon 28, Inc.
P51-926-2002
In Commercial Distribution

  • 00889795146120 ()
P51-926-2002

  • Surgical drill guide, reusable
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