Home GUDID 00849777004749 ProSpace™ DBM Moldable Putty (Jar)
Primary DI 00849777004749
Brand ProSpace™ DBM Moldable Putty (Jar)
Company Xtant Medical Holdings, Inc.
Model ME916
Device description 10.0cc
Published 2016-10-18
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) MQV Filler, Bone Void, Calcium Compound
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) Orthopedic 2 MQV Filler, Bone Void, Calcium Compound Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00849777004749 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00849777004749 00849777004749 849777004749 0849777004749
GMDN Terms# Term, Definition table Term Definition Human-derived demineralized bone matrix implant An 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.
Regulatory Flags# DUNS number 081224143 Device count 1 DM exempt false Premarket exempt false HCT/P true Kit false Combination product true Lot or batch true Serial number true Manufacturing date on label false Expiration date on label true Donation ID number true Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00840311258185 Fusion Lateral Instrument Set 38-SLAPHAMMER 2026-10-23 M697X06402401 Xpress Minimally Invasive Pedicle Screw System X064-0240 2026-10-14 M697X07300151 Xpress Minimally Invasive Pedicle Screw System X073-0015 2026-10-14 M697X07300251 Xpress Minimally Invasive Pedicle Screw System X073-0025 2026-10-14 M697X07300261 Xpress Minimally Invasive Pedicle Screw System X073-0026 2026-10-14 M697X07300271 Xpress Minimally Invasive Pedicle Screw System X073-0027 2026-10-14 M697X07300291 Xpress Minimally Invasive Pedicle Screw System X073-0029 2026-10-14 M697X073825100DL1 Xpress Minimally Invasive Pedicle Screw System X073-825100-DL 2026-10-14 M697X07382560DL1 Xpress Minimally Invasive Pedicle Screw System X073-82560-DL 2026-10-14 M697X07382565DL1 Xpress Minimally Invasive Pedicle Screw System X073-82565-DL 2026-10-14 M697X07382570DL1 Xpress Minimally Invasive Pedicle Screw System X073-82570-DL 2026-10-14 M697X07382575DL1 Xpress Minimally Invasive Pedicle Screw System X073-82575-DL 2026-10-14 M697X07382580DL1 Xpress Minimally Invasive Pedicle Screw System X073-82580-DL 2026-10-14 M697X07382585DL1 Xpress Minimally Invasive Pedicle Screw System X073-82585-DL 2026-10-14 M697X07382590DL1 Xpress Minimally Invasive Pedicle Screw System X073-82590-DL 2026-10-14 M697X07382595DL1 Xpress Minimally Invasive Pedicle Screw System X073-82595-DL 2026-10-14 00849777014144 Vesuvius Flowable DBM, 1cc 4104-K5010DP 2026-09-14 00849777014151 Vesuvius Flowable DBM, 2.5cc 4104-K5025DP 2026-09-14 00849777014168 Vesuvius Flowable DBM, 5cc 4104-K5050DP 2026-09-14 00849777014175 Vesuvius Flowable DBM, 10cc 4104-K5100DP 2026-09-14
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