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

    HERNIASTAT

    K Number: K884404 · Decision Nov 8, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    76
    Registration Numbers
    76
    Same Product Code
    41
    Applicant Total
    2
    Review Days
    20

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    HERNIASTAT
    K Number
    K884404
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Innovative Surgical Devices Corp.
    Date Received
    October 19, 1988
    Decision Date
    November 8, 1988
    Product Code
    GAG
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GAG Stapler, Surgical

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (GAG), ordered by most recent decision date.

    AEON™ Endoscopic Powered Stapler

    FDA 510(k)
    FDA Class 2 ·General Hospital

    da Vinci SP SureForm 45 Staplers and Reloads (SP1098)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AEON Endoscopic Powered Stapler (Short/AEPH060); AEON Endoscopic Powered Stapler (Medium/AEPH160); AEON Endoscopic Powered Stapler (Long/AEPH260)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GIA™ Stapler with Tri-Staple™ Technology

    FDA 510(k)
    FDA Class 2 ·General Hospital
    View all

    Other Clearances by Innovative Surgical Devices Corp.

    K Number Device Name
    K926337 BONE LAVAGE SYSTEM