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

    ACE 100 DEGREES TUBULAR PLATE

    K Number: K920738 · Decision Jul 27, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    519
    Registration Numbers
    519
    Same Product Code
    1313
    Applicant Total
    14
    Review Days
    159

    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
    ACE 100 DEGREES TUBULAR PLATE
    K Number
    K920738
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3030
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Ace Orthopedic Manufacturing Co.
    Date Received
    February 19, 1992
    Decision Date
    July 27, 1992
    Product Code
    HRS
    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
    HRS Plate, Fixation, Bone

    Similar 510(k) Clearances

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

    I.T.S. Clavicle Plates with Angular Stability; I.T.S. Volar Radius Plate with Angular Stability; I.T.S. Humeral Head Plate with Angular Stability; I.T.S. FR.O.H. Calcaneus Repair System; I.T.S. Pilonplate with Angular Stability; I.T.S. Olecranonplate with Angular Stability; I.T.S. Straight Plate with Angular Stability; I.T.S. Screw System; I.T.S. PRS Sacral Rod System; I.T.S. Fibula Plate PROlock with Angular Stability; I.T.S. Distal Humeral Plates with Angular Stability; I.T.S. LRS (L

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Exalta Proximal Tibia Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APTUS Clavicle System 2.8

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Pectus Blu System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Xpert PFP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Avanti Distal Elbow ORIF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic
    View all

    Other Clearances by Ace Orthopedic Manufacturing Co.

    K Number Device Name
    K934643 ACE HUMERAL NAIL
    K934962 AIM SUPRACONDYLAR NAIL
    K936045 ACE UNILATERAL FIXATOR II
    K926047 ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW
    K813554 ACE/KYLE CAPTURED HIP SCREW
    K810193 TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG
    K801594 ACE FISCHER EXTERNAL FIXATION DEVICE
    K791466 ACE EXTERNAL BONE CLAMP PART #S11
    K781839 BONE CLAMP, ACE EXTERNAL
    K781840 EXTERNAL ARTICULATION
    Search all 14 clearances from Ace Orthopedic Manufacturing Co. →