Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K251863
    Device Name
    CustomSurg OrthoPlanner
    Manufacturer
    CustomSurg AG
    Date Cleared
    2025-07-07

    (20 days)

    Product Code
    LLZ
    Regulation Number
    892.2050
    Why did this record match?
    Applicant Name (Manufacturer) :

    CustomSurg AG

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question

    Page 1 of 1