BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    TOWNLEY ALL POLY ACETABULAR CUP

    K Number: K952731 · Decision Dec 28, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    227
    Registration Numbers
    227
    Same Product Code
    562
    Applicant Total
    9
    Review Days
    196

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    Basic Information

    Device Name
    TOWNLEY ALL POLY ACETABULAR CUP
    K Number
    K952731
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3350
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biologically Oriented Prostheses
    Date Received
    June 15, 1995
    Decision Date
    December 28, 1995
    Product Code
    JDI
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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    Other Clearances by Biologically Oriented Prostheses

    K Number Device Name
    K002325 WUJIN #3 TIBIAL NAIL
    K992144 BIOPRO RIMMED ACETABULAR COMPOMENT
    K964472 RIOPRO COBALT TRAPEZIOMETARCARPAL RESURFACING COMPONENT
    K962769 HORIZON HIP SYSTEM
    K955916 TOWNLEY TOTAL ELBOW SYSTEM
    K954768 BIOPRO HEMI-ENDO MODULAR CERAMIC HEAD
    K953045 BIOPRO HEMI-ENDO MODULAR CERAMIC HEAD
    K951356 VARIOUS UHMWP HIP & KNEE JOINT PROSTHESIS MODIFIED