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

    CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS

    K Number: K090560 · Decision Jun 29, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    266
    Registration Numbers
    266
    Same Product Code
    279
    Applicant Total
    21
    Review Days
    119

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    Basic Information

    Device Name
    CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYS
    K Number
    K090560
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    880.6850
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Conmed Linvatec
    Date Received
    March 2, 2009
    Decision Date
    June 29, 2009
    Product Code
    KCT
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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    K092898 CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES
    K083161 ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)
    K080531 CONMED LINVATEC MICROFRACTURE INSTRUMENT STERILIZATION TRAY
    K072291 CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR
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    Search all 21 clearances from Conmed Linvatec →