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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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BioSet® - 00854095006498

DBM Paste
Rti Surgical, Inc.
008890
In Commercial Distribution

  • 00854095006498 ()
008890

  • Bone matrix implant, human-derived

BioSet® - 00854095006481

DBM Paste
Rti Surgical, Inc.
008850
In Commercial Distribution

  • 00854095006481 ()
008850

  • Bone matrix implant, human-derived

BioSet® - 00854095006474

DBM Paste
Rti Surgical, Inc.
007891
In Commercial Distribution

  • 00854095006474 ()
007891

  • Bone matrix implant, human-derived

BioSet® - 00854095006467

DBM Paste
Rti Surgical, Inc.
007890
In Commercial Distribution

  • 00854095006467 ()
007890

  • Bone matrix implant, human-derived

BioSet® - 00854095006450

DBM Paste
Rti Surgical, Inc.
007875
In Commercial Distribution

  • 00854095006450 ()
007875

  • Bone matrix implant, human-derived

BioSet® - 00854095006443

DBM Paste
Rti Surgical, Inc.
007845
In Commercial Distribution

  • 00854095006443 ()
007845

  • Bone matrix implant, human-derived

BioSet® - 00854095006436

DBM Paste
Rti Surgical, Inc.
007830
In Commercial Distribution

  • 00854095006436 ()
007830

  • Bone matrix implant, human-derived

BioSet® - 00854095006429

DBM Paste
Rti Surgical, Inc.
007820
In Commercial Distribution

  • 00854095006429 ()
007820

  • Bone matrix implant, human-derived

BioSet® - 00854095006412

DBM Paste
Rti Surgical, Inc.
006820
In Commercial Distribution

  • 00854095006412 ()
006820

  • Bone matrix implant, human-derived

BioSet® - 00854095006405

DBM Paste
Rti Surgical, Inc.
006810
In Commercial Distribution

  • 00854095006405 ()
006810

  • Bone matrix implant, human-derived
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