FDA 510(k) Applications Submitted by DENISE DAUGERT

FDA 510(k) Number Submission Date Device Name Applicant
K081044 04/14/2008 REJUVENATE MODULAR HIP SYSTEM HOWMEDICA OSTEONICS CORP
K191414 05/28/2019 EXETER Centralizer, EXETER 2.5mm Plug Stryker Orthopaedics
K142462 09/02/2014 Restoration Anatomic Shell STRYKER ORTHOPAEDICS
K082892 09/30/2008 REJUVENATE MONOLITHIC HIP SYSTEM HOWMEDICA OSTEONICS CORP
K143085 10/27/2014 Stryker Orthopaedics Acetabular Shells, Femoral Stems and Total Hip Instruments for use with the Direct Superior Approach STRYKER ORTHOPAEDICS


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