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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DBX Putty, 10cc
Musculoskeletal Transplant Foundation, Inc.
038100
In Commercial Distribution

  • W4184038100T0473 ()

  • 10 cc volume
038100

  • Bone matrix implant, human-derived
DBX Putty, 5cc
Musculoskeletal Transplant Foundation, Inc.
038050
In Commercial Distribution

  • W4184038050T0473 ()

  • 5 cc volume
038050

  • Bone matrix implant, human-derived
DBX Putty, 2.5cc
Musculoskeletal Transplant Foundation, Inc.
038025
In Commercial Distribution

  • W4184038025T0473 ()

  • 2.5 cc volume
038025

  • Bone matrix implant, human-derived
DBX Putty, 1cc
Musculoskeletal Transplant Foundation, Inc.
038010
In Commercial Distribution

  • W4184038010T0473 ()

  • 1.0 cc volume
038010

  • Bone matrix implant, human-derived
QuickGraft Pre-Sutured Tendon
Musculoskeletal Transplant Foundation, Inc.
430PST
In Commercial Distribution

  • W41844300PSTT165 ()
430PST

  • Tendon graft
DBX Putty 1cc
Musculoskeletal Transplant Foundation, Inc.
428010
In Commercial Distribution

  • W4184428010T0473 ()

  • 1 cc volume
428010

  • Bone matrix implant, human-derived
Legacy DBM, 10CC
Musculoskeletal Transplant Foundation, Inc.
420810
In Commercial Distribution

  • W4184420810T0473 ()

  • 1.0 cc volume
420810

  • Bone matrix implant, human-derived
Legacy DBM, 2.5CC
Musculoskeletal Transplant Foundation, Inc.
420802
In Commercial Distribution

  • W4184420802T0473 ()

  • 1.0 cc volume
420802

  • Bone matrix implant, human-derived
Legacy DBM, 1CC
Musculoskeletal Transplant Foundation, Inc.
420801
In Commercial Distribution

  • W4184420801T0473 ()

  • 1.0 cc volume
420801

  • Bone matrix implant, human-derived
Legacy DBM, 0.5cc
Musculoskeletal Transplant Foundation, Inc.
420800
In Commercial Distribution

  • W4184420800T0473 ()

  • 1.0 cc volume
420800

  • Bone matrix implant, human-derived
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