BEUDAMED
    Product Code: KAN FDA class 1 21 CFR 878.4800

    Chisel, Nasal

    General, Plastic Surgery

    A nasal chisel is a surgical instrument used in rhinoplasty and septoplasty procedures to cut, shape, or remodel nasal bone and cartilage structures. It is classified as an FDA Class 1 device, the lowest risk category, subject to general controls only and not requiring premarket clearance. Product code KAN is regulated under 21 CFR 878.4800 in the General, Plastic Surgery medical specialty. No special flags apply to this device.

    View on FDA
    510(k)s
    0
    FEI Numbers
    70
    Registration Numbers
    70
    Unique Applicants
    0
    Years Active
    —

    Basic Information

    Product Code
    KAN
    Device Class
    FDA class 1
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Review Panel
    SU
    Submission Type
    4

    Device Characteristics

    ✗
    GMP Exempt
    ✗
    Implant
    ✗
    Life Sustain/Support
    ✗
    Third Party
    —
    Summary Malfunction Reporting

    FEI Numbers

    This FDA classification entry is associated with 70 FEI numbers. Click on an entry to view related FDA registrations.

    Registration Numbers

    This FDA classification entry is associated with 70 registration numbers. Click on an entry to view related FDA registrations.