BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AlloFuse Plus Putty

    Reg #: 3000215346 · FEI: 3000215346 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    9
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    ALLOSOURCE
    Registration Number
    3000215346
    FEI Number
    3000215346
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6278 S Troy Circle
    City
    Centennial
    State
    CO
    ZIP
    80111
    Country
    US

    Regulatory Submissions

    510(k) Number
    K103036

    Owner / Operator

    Firm Name
    AlloSource
    Operator Number
    10025681
    Address
    6278 South Troy Circle
    City
    Centennial
    State
    CO
    Postal Code
    80111
    Country
    US

    Products

    Device Name Product Code
    Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) MBP
    Filler, Bone Void, Calcium Compound MQV

    Proprietary Names

    AlloFuse Plus Putty HERO DBM Plus Paste NuVasive Propel DBM Putty Plus HERO DBM Plus Putty StimuBlast CB Paste StimuBlast CB Putty NuVasive Propel DBM Gel Plus AlloFuse Plus Paste BiomaX Bone Graft Putty Plus Chips

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device