BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Calvary Lumbar Interbody Spacers/ Fusion Device (crescent & straight-shaped interbody cages; 7-15mm heights)

    Reg #: 3007279845 · FEI: 3007279845 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    CALVARY SPINE, LLC
    Registration Number
    3007279845
    FEI Number
    3007279845
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    308 North Wind Rd.
    City
    Towson
    State
    MD
    ZIP
    21204
    Country
    US

    Regulatory Submissions

    510(k) Number
    K082260

    Owner / Operator

    Firm Name
    Calvary Spine, LLC
    Operator Number
    10027607
    Address
    308 North Wind Rd.
    City
    Towson
    State
    MD
    Postal Code
    21204
    Country
    US

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX
    Intervertebral Fusion Device With Bone Graft, Cervical ODP

    Proprietary Names

    Calvary Lumbar Interbody Spacers/ Fusion Device (crescent & straight-shaped interbody cages; 7-15mm heights) Calvary Cervical Interbody Spacers/ Fusion Device (standard & large footprint interbody cages; 5-9mm heights)

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility