AccessGUDID - DEVICE: Legacy DBM (W4184420810T0473)

GUDID

Device Identifier (DI) Information

Brand Name: Legacy DBM
Version or Model: 420810
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 420810
Company Name: Musculoskeletal Transplant Foundation, Inc.

Primary DI Number: W4184420810T0473
Issuing Agency: ICCBBA
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 187560545 *Terms of Use

Device Description: Legacy DBM, 10CC

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	Yes

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
47257	Bone matrix implant, human-derived	An sterile implantable device made primarily of human demineralized bone matrix (DBM) (acid extraction of allogeneic bone resulting in loss of most of the mineralized component but retention of proteins) intended to fill bony voids or gaps caused by trauma or surgery, including use in the maxillofacial and/or mandibular bone. The device is bioabsorbable, osteoconductive, and has demonstrated at least potential osteoinductivity for the stimulation of new bone growth. The DBM may be combined with various carrier compounds (e.g., gelatin, hydrogel, starch) or other materials. It is available in the form of powder, crushed granules, putty, chips, or a gel that can be injected through a syringe.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
MQV	Filler, Bone Void, Calcium Compound
GXP	Methyl Methacrylate For Cranioplasty

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 1.0 cc volume

Device Record Status

Public Device Record Key: f85254b8-1ba1-45ad-86fe-94394db3b4f7
Public Version Date: July 11, 2022
Public Version Number: 1
DI Record Publish Date: July 01, 2022