BEUDAMED
    FDA Registration Active 🇺🇸 United States

    TJO - Tibial Insert, CR/Congruent, Std Poly (5300.XX.XXX), Device Listing: D178113

    Reg #: 3009882462 · FEI: 3009882462 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PERRYMAN COMPANY
    Registration Number
    3009882462
    FEI Number
    3009882462
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    149 S Johnson Rd
    City
    Houston
    State
    PA
    ZIP
    15342
    Country
    US

    Regulatory Submissions

    510(k) Number
    K112906

    Owner / Operator

    Firm Name
    Perryman Company
    Operator Number
    10042198
    Address
    149 South Johnson Rd
    City
    Houston
    State
    PA
    Postal Code
    15342
    Country
    US
    Correspondent
    Dylan Crawford

    Products

    Device Name Product Code
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer JWH

    Proprietary Names

    TJO - Tibial Insert, CR/Congruent, Std Poly (5300.XX.XXX), Device Listing: D178113 TJO - Dome Extension (5601000), Device Listing: D178113 TJO - Tibial Insert, Ultra-PS, Std Poly, (5301X.XXX), Device Listing: D178113 TJO - TIBIAL INSERT SET SCREW (5603000), Device Listing: D178113 TJO - TIBIAL BASEPLATE, NONPOROUS (5201.XX.XXX), Device Listing: D178113 TJO - Domed Patella, (5500.XX.XXX), Device Listing: D178113 TJO - Tibial Insert Set Screw (5602000), Device Listing: D178113 TJO - Tibial Insert, Ultra-PS, Std Poly (5301.XX.XXX), Device Listing: D178113

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)