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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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Propel - 00887517971531

Propel DBM Gel Plus, 1cc
Nuvasive, Inc.
5020401
In Commercial Distribution

  • 00887517971531 ()


  • Bone matrix implant, human-derived

Propel - 00887517971517

Propel DBM Gel, 10cc
Nuvasive, Inc.
5020310
In Commercial Distribution

  • 00887517971517 ()


  • Bone matrix implant, human-derived

Propel - 00887517970497

Propel DBM Gel, 5cc
Nuvasive, Inc.
5020305
In Commercial Distribution

  • 00887517970497 ()


  • Bone matrix implant, human-derived

Propel - 00887517970480

Propel DBM Gel, 1cc OUS
Nuvasive, Inc.
5020301994
In Commercial Distribution

  • 00887517970480 ()


  • Bone matrix implant, human-derived

Propel - 00887517970473

Propel DBM Gel, 1cc
Nuvasive, Inc.
5020301
In Commercial Distribution

  • 00887517970473 ()


  • Bone matrix implant, human-derived

Propel - 00887517970466

Propel DBM Putty Plus, 10cc OUS
Nuvasive, Inc.
5020210994
In Commercial Distribution

  • 00887517970466 ()


  • Bone matrix implant, human-derived

Propel - 00887517970459

Propel DBM Putty Plus, 10cc
Nuvasive, Inc.
5020210
In Commercial Distribution

  • 00887517970459 ()


  • Bone matrix implant, human-derived

Propel - 00887517970442

Propel DBM Putty Plus, 5cc OUS
Nuvasive, Inc.
5020205994
In Commercial Distribution

  • 00887517970442 ()


  • Bone matrix implant, human-derived

Propel - 00887517970435

Propel DBM Putty Plus, 5cc
Nuvasive, Inc.
5020205
In Commercial Distribution

  • 00887517970435 ()


  • Bone matrix implant, human-derived

Propel - 00887517971562

Propel DBM Gel Plus, 3cc OUS
Nuvasive, Inc.
5020403994
In Commercial Distribution

  • 00887517971562 ()


  • Bone matrix implant, human-derived
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