SEARCH RESULTS FOR: (*purchase New Brunswick driver*)(704881 results)

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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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RTI Allograft Paste - 00898623002002

Allograft Paste 1cc
Rti Surgical, Inc.
801201
In Commercial Distribution

  • 00898623002002 ()


  • Bone matrix implant, human-derived

Propel - 00887517614384

Propel Putty, Large
Nuvasive, Inc.
5020010
In Commercial Distribution

  • 00887517614384 ()


  • Bone matrix implant, human-derived

Propel - 00887517614377

Propel Putty, Medium
Nuvasive, Inc.
5020005
In Commercial Distribution

  • 00887517614377 ()


  • Bone matrix implant, human-derived

Propel - 00887517614360

Propel Putty, Small
Nuvasive, Inc.
5020001
In Commercial Distribution

  • 00887517614360 ()


  • Bone matrix implant, human-derived

Propel - 00887517971586

Propel DBM Gel Plus, 8cc OUS
Nuvasive, Inc.
5020408994
In Commercial Distribution

  • 00887517971586 ()


  • Bone matrix implant, human-derived

Propel - 00887517971579

Propel DBM Gel Plus, 8cc
Nuvasive, Inc.
5020408
In Commercial Distribution

  • 00887517971579 ()


  • 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

Propel - 00887517971555

Propel DBM Gel Plus, 3cc
Nuvasive, Inc.
5020403
In Commercial Distribution

  • 00887517971555 ()


  • Bone matrix implant, human-derived

Propel - 00887517971548

Propel DBM Gel Plus, 1cc OUS
Nuvasive, Inc.
5020401994
In Commercial Distribution

  • 00887517971548 ()


  • Bone matrix implant, human-derived

Propel - 00887517971531

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

  • 00887517971531 ()


  • Bone matrix implant, human-derived
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