BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AltiVate Reverse Glenoid Peripheral Drill Guide

    Reg #: 1644408 · FEI: 1000116912 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    13
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    ENCORE MEDICAL, L.P.
    Registration Number
    1644408
    FEI Number
    1000116912
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    9800 METRIC BLVD.
    City
    AUSTIN
    State
    TX
    ZIP
    78758
    Country
    US

    Regulatory Submissions

    510(k) Number
    K233481

    Owner / Operator

    Firm Name
    ENCORE MEDICAL, L.P.
    Operator Number
    9002203
    Address
    9800 METRIC BLVD., --
    City
    Austin
    State
    TX
    Postal Code
    78758
    Country
    US
    Correspondent
    Sherri - Mellingen

    Products

    Device Name Product Code
    Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented KWS
    Shoulder Prosthesis, Reverse Configuration PHX

    Proprietary Names

    AltiVate Reverse Glenoid Peripheral Drill Guide AltiVate Reverse Glenoid Hood Rasp AltiVate Reverse Glenoid Cannulated Boss Drill AltiVate Reverse® Glenoid AltiVate Reverse Wedge Glenoid Reamer Boss Drill AltiVate Reverse Wedge Glenoid Reamer Head AltiVate Reverse Glenoid Peripheral Drill/Screw Guide Replacement Thumbscrew AltiVate Reverse Glenoid Hood Rasp Guide AltiVate Reverse Cannulated Glenoid Reamer AltiVate Reverse Glenoid Baseplate Inserter ALTIVATE REVERSE GLENOID ANGLED REAMER AltiVate Reverse Glenoid Baseplate Rim Planer AltiVate Reverse Wedge Glenoid Reamer Sleeve

    Establishment Types

    Manufacture Medical Device